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Qin Wang, Jian Hu, Panpan Bian, Chi Chen, Yanli Wang, Shihong Cheng, Yufen Guo & Baicheng Xu. (2023) The effect of SLC26A4 gene mutations on long-term rehabilitative outcomes in cochlear implant patients. Acta Oto-Laryngologica 143:2, pages 156-162.
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Meng Zhang, Yuechen Han, Fengguo Zhang, Xiaohui Bai & Haibo Wang. (2019) Mutation spectrum and hotspots of the common deafness genes in 314 patients with nonsyndromic hearing loss in Heze area, China. Acta Oto-Laryngologica 139:7, pages 612-617.
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S. M. Yang, Ying Liu, C. Liu, A. H. Yin, Y. F. Wu, X. E. Zheng, H. M. Yang & J. Yang. (2018) Hearing-loss-associated gene detection in neonatal intensive care unit. The Journal of Maternal-Fetal & Neonatal Medicine 31:3, pages 284-288.
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Yalin Ma, Yun Xiao, Xiaohui Bai, Fengguo Zhang, Daogong Zhang, Xinmao Xu, Lei Xu & Haibo Wang. (2016) GJB2, SLC26A4, and mitochondrial DNA12S rRNA hot-spots in 156 subjects with non-syndromic hearing loss in Tengzhou, China. Acta Oto-Laryngologica 136:8, pages 800-805.
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Shujing Han, Xiaojian Yang, Yi Zhou, Jinsheng Hao, Adong Shen, Fang Xu, Ping Chu, Yaqiong Jin, Jie Lu, Yongli Guo, Jin Shi, Haihong Liu & Xin Ni. (2016) Deafness gene mutations in newborns in Beijing. Acta Oto-Laryngologica 136:5, pages 475-479.
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Yi-Ming Zhu, Yong Li, Yan-Li Wang, Pan-Pan Bian, Bai-Cheng Xu, Xiao-Wen Liu, Xing-Jian Chen, Feng Liu, Yu-Fen Guo & Qiu-Ju Wang. (2015) The deafness-causing mutation c.508_511dup in the GJB2 gene and a literature review. Acta Oto-Laryngologica 135:9, pages 914-918.
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Shi-Hong Duan, Yi-Ming Zhu, Yan-Li Wang & Yu-Fen Guo. (2015) Common molecular etiology of nonsyndromic hearing loss in 484 patients of 3 ethnicities in northwest China. Acta Oto-Laryngologica 135:6, pages 586-591.
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Bai-Cheng Xu, Pan-Pan Bian, Xiao-Wen Liu, Yi-Ming Zhu, Xiao-Long Yang, Jian-Li Ma, Xing-Jian Chen, Yan-Li Wang & Yu-Fen Guo. (2014) Analysis of common deafness gene mutations in deaf people from unique ethnic groups in Gansu Province, China. Acta Oto-Laryngologica 134:9, pages 924-929.
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Wan Du, Yi Ming Zhu, Yu Fen Guo, Qiu Ju Wang & Xiao Wen Liu. (2014) Prevalence of GJB2 mutations in the Silk Road region of China and a report of three novel variants. Acta Oto-Laryngologica 134:4, pages 373-381.
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Xiao-Long Yang, Xu Bai-Cheng, Xing-Jian Chen, Bian Pan-Pan, Ma Jian-Li, Liu Xiao-Wen, Zhe-Wen Zhang, Du Wan, Yi-Ming Zhu & Yu-Fen Guo. (2013) Common molecular etiology of patients with nonsyndromic hearing loss in Tibetan, Tu nationality, and Mongolian patients in the northwest of China. Acta Oto-Laryngologica 133:9, pages 930-934.
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Yu-bin Ji, Dong-Yi Han, Lan Lan, Da-Yong Wang, Liang Zong, Fei-Fan Zhao, Qiong Liu, Cindy Benedict-Alderfer, Qing-yin Zheng & Qiu-Ju Wang. (2011) Molecular epidemiological analysis of mitochondrial DNA12SrRNA A1555G, GJB2, and SLC26A4 mutations in sporadic outpatients with nonsyndromic sensorineural hearing loss in China. Acta Oto-Laryngologica 131:2, pages 124-129.
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Geir Siem, Toril Fagerheim, Christoffer Jonsrud, Claude Laurent, Erik Teig, Sten Harris, Trond P. Leren, Andreas Früh & Ketil Heimdal. (2010) Causes of hearing impairment in the Norwegian paediatric cochlear implant program. International Journal of Audiology 49:8, pages 596-605.
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Articles from other publishers (57)
Qing-Qing Jiang, Juan-Juan Zhu, Shu-Ling Fan, Ya-Ping Hou, Xie-Ying Hu, Jie Shi, Lei Wu & Ying Luo. (2024) Establishment and application of a reverse dot blot assay for 13 mutations of hearing-loss genes in primary hospitals in China. Asian Biomedicine 18:1, pages 11-17.
Crossref
Crossref
Leonid A. Klarov, Vera G. Pshennikova, Georgii P. Romanov, Aleksandra M. Cherdonova, Aisen V. Solovyev, Fedor M. Teryutin, Nikolay V. Luginov, Petr M. Kotlyarov & Nikolay A. Barashkov. (2022) Analysis of SLC26A4, FOXI1, and KCNJ10 Gene Variants in Patients with Incomplete Partition of the Cochlea and Enlarged Vestibular Aqueduct (EVA) Anomalies. International Journal of Molecular Sciences 23:23, pages 15372.
Crossref
Crossref
Panpan Bian, Baicheng Xu, Xiaoyun Zhao, YiMing Zhu, Chi Chen, XingJian Chen, Xiaowen Liu, Yanli Wang & Yufen Guo. (2022) Analysis of GJB2 Gene Mutations in 1330 Deafness Cases of Major Ethnic Groups in Northwest China. INQUIRY: The Journal of Health Care Organization, Provision, and Financing 59, pages 004695802110555.
Crossref
Crossref
Valeriia Yu. Danilchenko, Marina V. Zytsar, Ekaterina A. Maslova, Marita S. Bady-Khoo, Nikolay A. Barashkov, Igor V. Morozov, Alexander A. Bondar & Olga L. Posukh. (2021) Different Rates of the SLC26A4-Related Hearing Loss in Two Indigenous Peoples of Southern Siberia (Russia). Diagnostics 11:12, pages 2378.
Crossref
Crossref
Shihong Duan, Yufen Guo, Xingjian Chen & Yong Li. (2021) Genetic mutations in patients with nonsyndromic hearing impairment of minority and Han Chinese ethnicities in Qinghai, China. Journal of International Medical Research 49:4, pages 030006052110008.
Crossref
Crossref
Mahbobeh KoohiyanMorteza Hashemzadeh-ChaleshtoriMohammad Amin Tabatabaiefar. (2021) Molecular diagnosis of <i>SLC26A4</i>-related hereditary hearing loss in a group of patients from two provinces of Iran. Intractable & Rare Diseases Research 10:1, pages 23-30.
Crossref
Crossref
Chen Zhou, Xiangman Zou, Cuiying Peng, Guoqiang Gao & Zifen Guo. (2020) A novel genotyping technique for discriminating LVAS-associated high-frequency variants in SLC26A4 gene. AMB Express 10:1.
Crossref
Crossref
Xiao-Wen Liu, Jian-Chao Wang, Su-Yang Wang, Shu-Juan Li, Yi-Ming Zhu, Wen-Juan Ding, Chen-Yang Xu, Lei Duan, Bai-Cheng Xu & Yu-Fen Guo. (2020) The mutation frequencies of GJB2, GJB3, SLC26A4 and MT-RNR1 of patients with severe to profound sensorineural hearing loss in northwest China. International Journal of Pediatric Otorhinolaryngology 136, pages 110143.
Crossref
Crossref
Maryam Najafi, Dor Mohammad Kordi-Tamandani, Farkhondeh Behjati, Simin Sadeghi-Bojd, Zeineb Bakey, Ehsan Ghayoor Karimiani, Isabel Schüle, Anoush Azarfar & Miriam Schmidts. (2019) Mimicry and well known genetic friends: molecular diagnosis in an Iranian cohort of suspected Bartter syndrome and proposition of an algorithm for clinical differential diagnosis. Orphanet Journal of Rare Diseases 14:1.
Crossref
Crossref
Jeon Mi Lee, Hyun Jin Lee, Jinsei Jung, In Seok Moon, Sung Huhn Kim, Jin Kim & Jae Young Choi. (2019) Lessons From an Analysis of Newborn Hearing Screening Data for Children With Cochlear Implants. Otology & Neurotology 40:9, pages e909-e917.
Crossref
Crossref
Mahbobeh koohiyan. (2019) A systematic review of SLC26A4 mutations causing hearing loss in the Iranian population. International Journal of Pediatric Otorhinolaryngology 125, pages 1-5.
Crossref
Crossref
Yongan Zhou, Chao Li, Min Li, Zhonghua Zhao, Shuxiong Tian, Hou Xia, Peixian Liu, Yaxin Han, Ruirui Ren, Jianping Chen, Caihong Jia & Wei Guo. (2019) Mutation analysis of common deafness genes among 1,201 patients with non‐syndromic hearing loss in Shanxi Province. Molecular Genetics & Genomic Medicine 7:3.
Crossref
Crossref
Andrew Schaefer, Albert Lim & Grainne Gorman. 2019. Diagnosis and Management of Mitochondrial Disorders. Diagnosis and Management of Mitochondrial Disorders
63
79
.
Jargalkhuu Erdenechuluun, Yin-Hung Lin, Khongorzul Ganbat, Delgermaa Bataakhuu, Zaya Makhbal, Cheng-Yu Tsai, Yi-Hsin Lin, Yen-Hui Chan, Chuan-Jen Hsu, Wei-Chung Hsu, Pei-Lung Chen & Chen-Chi Wu. (2018) Unique spectra of deafness-associated mutations in Mongolians provide insights into the genetic relationships among Eurasian populations. PLOS ONE 13:12, pages e0209797.
Crossref
Crossref
Pingsen Zhao, Lifang Lin & Liubing Lan. (2018) Analysis of mutation spectrum of common deafness-causing genes in Hakka newborns in southern China by semiconductor sequencing. Medicine 97:38, pages e12285.
Crossref
Crossref
Bangqing Huang, Mingyu Han, Guojian Wang, ShaSha Huang, Jialing Zeng, Yongyi Yuan & Pu Dai. (2018) Genetic mutations in non-syndromic deafness patients in Hainan Province have a different mutational spectrum compared to patients from Mainland China. International Journal of Pediatric Otorhinolaryngology 108, pages 49-54.
Crossref
Crossref
Chao Wang, Shengzhou Wang, Hongyan Chen & Daru Lu. (2018) Establishment of a Gene Detection System for Hotspot Mutations of Hearing Loss. BioMed Research International 2018, pages 1-8.
Crossref
Crossref
Jianfen Luo, Xiaohui Bai, Fengguo Zhang, Yun Xiao, Lintao Gu, Yuechen Han, Zhaomin Fan, Jianfeng Li, Lei Xu & Haibo Wang. (2017) Prevalence of Mutations in Deafness‐Causing Genes in Cochlear Implanted Patients with Profound Nonsyndromic Sensorineural Hearing Loss in Shandong Province, China. Annals of Human Genetics 81:6, pages 258-266.
Crossref
Crossref
Jing Pan, Ping Xu, Weibo Tang, Zhongtao Cui, Miao Feng & Chunying Wang. (2017) Mutation analysis of common GJB2 , SCL26A4 and 12S rRNA genes among 380 deafness patients in northern China. International Journal of Pediatric Otorhinolaryngology 98, pages 39-42.
Crossref
Crossref
Shi-Hong Duan, Jian-Li Ma, Xiao-Long Yang & Yu-Fen Guo. (2017) Simultaneous multi-gene mutation screening using SNPscan in patients from ethnic minorities with nonsyndromic hearing-impairment in Northwest China. Molecular Medicine Reports 16:5, pages 6722-6728.
Crossref
Crossref
Xudong Wang, Yongjun Hong, Peihong Cai, Ning Tang, Ying Chen, Tizhen Yan, Yinghua Liu, Qiuying Huang & Qingge Li. (2017) Rapid and Reliable Detection of Nonsyndromic Hearing Loss Mutations by Multicolor Melting Curve Analysis. Scientific Reports 7:1.
Crossref
Crossref
Mingming Wang, Fengguo Zhang, Lei Xu, Yun Xiao, Jianfeng Li, Zhaomin Fan, Qian Sun, Xiaohui Bai & Haibo Wang. (2016) Novel compound heterozygous mutations in SLC26A4 gene in a Chinese Han family with enlarged vestibular aqueduct. International Journal of Pediatric Otorhinolaryngology 90, pages 170-174.
Crossref
Crossref
Bo Gyung Kim, Kyung Jin Roh, Ah Young Park, Seung Chul Lee, Bo Sung Kang, Young Joon SeoJong Dae Lee & Jae Young Choi. (2015)
Early deterioration of residual hearing in patients with
SLC
26
A
4
mutations
. The Laryngoscope 126:8.
Crossref
Crossref
Joseph FosterIIII & Mustafa Tekin. (2016) Aminoglycoside induced ototoxicity associated with mitochondrial DNA mutations. Egyptian Journal of Medical Human Genetics 17:3, pages 287-293.
Crossref
Crossref
Fengguo Zhang, Xiaohui Bai, Yun Xiao, Xue Zhang, Guodong Zhang, Jianfeng Li, Lei Xu & Haibo Wang. (2016) Identification of a novel mutation in SLC26A4 gene in a Chinese family with enlarged vestibular aqueduct syndrome. International Journal of Pediatric Otorhinolaryngology 85, pages 75-79.
Crossref
Crossref
Wen-xia Chen, Yue Huang, Xiao-lin Yang, Bo Duan, Ping Lu, Yan Wang & Zheng-min Xu. (2016) The homozygote p.V27I/p.E114G variant of GJB2 is a putative indicator of nonsyndromic hearing loss in Chinese infants. International Journal of Pediatric Otorhinolaryngology 84, pages 48-51.
Crossref
Crossref
Yalin Ma, Yun Xiao, Fengguo Zhang, Yuechen Han, Jianfeng Li, Lei Xu, Xiaohui Bai & Haibo Wang. (2016) Novel compound heterozygous mutations in MYO7A gene associated with autosomal recessive sensorineural hearing loss in a Chinese family. International Journal of Pediatric Otorhinolaryngology 83, pages 179-185.
Crossref
Crossref
Bidisha Adhikary, Sudakshina Ghosh, Silpita Paul, Biswabandhu Bankura, Arup Kumar Pattanayak, Subhradev Biswas, Biswanath Maity & Madhusudan Das. (2015) Spectrum and frequency of GJB2, GJB6 and SLC26A4 gene mutations among nonsyndromic hearing loss patients in eastern part of India. Gene 573:2, pages 239-245.
Crossref
Crossref
Yi Jiang, Shasha Huang, Tao Deng, Lihua Wu, Juan Chen, Dongyang Kang, Xiufeng Xu, Ruiyu Li, Dongyi Han & Pu Dai. (2015) Mutation Spectrum of Common Deafness-Causing Genes in Patients with Non-Syndromic Deafness in the Xiamen Area, China. PLOS ONE 10:8, pages e0135088.
Crossref
Crossref
Keita Tsukada, Shin-ya Nishio, Mitsuru Hattori & Shin-ichi Usami. (2015)
Ethnic-Specific Spectrum of
GJB2
and
SLC26A4
Mutations
. Annals of Otology, Rhinology & Laryngology 124:1_suppl, pages 61S-76S.
Crossref
Crossref
Wu Jing, Hao Zongjie, Fu Denggang, Hei Na, Zhang Bin, Zhou Aifen, Hu Xijiang, Yao Cong, Dong Yunping, Huijun Z Ring & Brian Z Ring. (2015) Mitochondrial mutations associated with aminoglycoside ototoxicity and hearing loss susceptibility identified by meta-analysis. Journal of Medical Genetics 52:2, pages 95-103.
Crossref
Crossref
Jie QingYuan ZhouRuosha LaiPeng HuYan DingWeijing WuZian XiaoPhi T. HoYuyuan LiuJia LiuLilin DuDenise YanBradley J. GoldsteinXuezhong LiuDinghua Xie. (2015)
Prevalence of Mutations in
GJB2
,
SLC26A4
, and
mtDNA
in Children with Severe or Profound Sensorineural Hearing Loss in Southwestern China
. Genetic Testing and Molecular Biomarkers 19:1, pages 52-58.
Crossref
Crossref
Kaitian Chen, Ling Zong, Min Liu, Xianren Wang, Wei Zhou, Yuan Zhan, Hui Cao, Chang Dong, Haocheng Tang & Hongyan Jiang. (2014) Developing regional genetic counseling for southern Chinese with nonsyndromic hearing impairment: a unique mutational spectrum. Journal of Translational Medicine 12:1.
Crossref
Crossref
Li Qian, Ji Yubin, Han Bing, Zong Liang, Lan Lan, Zhao Yali, Wang Hongyang, Wang Dayong & Wang Qiuju. (2014) Comparative study of mutation spectrums of MT-RNR1 m.1555A>G, GJB2, and SLC26A4 between familial and sporadic patients with nonsyndromic sensorineural hearing loss in Chinese Han. Chinese Medical Journal 127:18, pages 3233-3237.
Crossref
Crossref
Dylan K. Chan & Kay W. Chang. (2014) GJB2-associated hearing loss: Systematic review of worldwide prevalence, genotype, and auditory phenotype. The Laryngoscope 124:2, pages E34-E53.
Crossref
Crossref
GEN-DONG YAO, SHOU-XIA LI, DING-LI CHEN, HAI-QIN FENG, SU-BIN ZHAO, YONG-JIE LIU, LI-LI GUO, ZHI-MING YANG, XIAO-FANG ZHANG, CAI-XIA SUN, ZE-HUI WANG & WEI-YONG ZHANG. (2014) Combination of hearing screening and genetic screening for deafness-susceptibility genes in newborns. Experimental and Therapeutic Medicine 7:1, pages 218-222.
Crossref
Crossref
Bo Gyung Kim. (2014)
SLC26A4
Mutations in Korean Population
. Korean Journal of Otorhinolaryngology-Head and Neck Surgery 57:11, pages 733.
Crossref
Crossref
Feng Xin, Yongyi Yuan, Xiaoming Deng, Mingyu Han, Guojian Wang, Jiandong Zhao, Xue Gao, Jun Liu, Fei Yu, Dongyi Han & Pu Dai. (2013) Genetic mutations in nonsyndromic deafness patients of Chinese minority and han ethnicities in Yunnan, China. Journal of Translational Medicine 11:1.
Crossref
Crossref
Hae-Mi Woo, Hong-Joon Park, Jeong-In Baek, Mi-Hyun Park, Un-Kyung Kim, Borum Sagong & Soo Kyung Koo. (2013) Whole-exome sequencing identifies MYO15A mutations as a cause of autosomal recessive nonsyndromic hearing loss in Korean families. BMC Medical Genetics 14:1.
Crossref
Crossref
Chun-Jui Huang, Tsun-Hsing Lei, Wei-Lun Chang, Tzong-Yang Tu, An-Suey Shiao, Chih-Yang Chiu & Tjin-Shing Jap. (2013) A Novel mutation in the SLC26A4 gene in a Chinese family with Pendred syndrome. International Journal of Pediatric Otorhinolaryngology 77:9, pages 1495-1499.
Crossref
Crossref
Joshua C. Yelverton, Kathleen Arnos, Xia‐Juan Xia, Walter E. Nance, Arti Pandya & Kelley M. Dodson. (2013) The Clinical and Audiologic Features of Hearing Loss Due to Mitochondrial Mutations. Otolaryngology–Head and Neck Surgery 148:6, pages 1017-1022.
Crossref
Crossref
Bo Gyung Kim, Joong-Wook Shin, Hong-Joon Park, Jung Min Kim, Un-Kyung Kim & Jae Young Choi. (2013) Limitations of hearing screening in newborns with PDS mutations. International Journal of Pediatric Otorhinolaryngology 77:5, pages 833-837.
Crossref
Crossref
Jun Yao, Yajie Lu, Qinjun Wei, Xin Cao & Guangqian Xing. (2012) A systematic review and meta-analysis of 235delC mutation of GJB2 gene. Journal of Translational Medicine 10:1.
Crossref
Crossref
Zhewen Zhang, Wenjuan Ding, Xiaowen Liu, Baicheng Xu, Wan Du, Shuling Nan & Yufen Guo. (2012) Auditory screening concurrent deafness predisposing genes screening in 10,043 neonates in Gansu province, China. International Journal of Pediatric Otorhinolaryngology 76:7, pages 984-988.
Crossref
Crossref
Yu Chen, Mayila Tudi, Jie Sun, Chao He, Hong-li Lu, Qing Shang, Di Jiang, Pilidong Kuyaxi, Bin Hu & Hua Zhang. (2011) Genetic mutations in non-syndromic deafness patients of uyghur and han chinese ethnicities in xinjiang, China: a comparative study. Journal of Translational Medicine 9:1.
Crossref
Crossref
Fei-Fan ZhaoYu-Bin JiDa-Yong WangLan LanMing-Kun HanQian LiYali ZhaoShaoqi RaoDongyi HanQiu-Ju Wang. (2011)
Phenotype–Genotype Correlation in 295 Chinese Deaf Subjects with Biallelic Causative Mutations in the
GJB2
Gene
. Genetic Testing and Molecular Biomarkers 15:9, pages 619-625.
Crossref
Crossref
Guanming Chen, Fang He, Siqing Fu & Jiashu Dong. (2011) GJB2 and mitochondrial DNA 1555A > G mutations in students with hearing loss in the Hubei Province of China. International Journal of Pediatric Otorhinolaryngology 75:9, pages 1156-1159.
Crossref
Crossref
Soo-Young Choi, Kyu Yup Lee, Hyun-Jin Kim, Hyo-Kyeong Kim, Qing Chang, Hong-Joon Park, Chang-Jin Jeon, Xi Lin, Jinwoong Bok & Un-Kyung Kim. (2011) Functional Evaluation of GJB2 Variants in Nonsyndromic Hearing Loss. Molecular Medicine 17:5-6, pages 550-556.
Crossref
Crossref
Qiu-Ju Wang, Ya-Li Zhao, Shao-Qi Rao, Yu-Fen Guo, Yao He, Lan Lan, Wei-Yan Yang, Qing-Yin Zheng, Robert J. Ruben, Dong-Yi Han & Yan Shen. (2011) Newborn hearing concurrent gene screening can improve care for hearing loss: A study on 14,913 Chinese newborns. International Journal of Pediatric Otorhinolaryngology 75:4, pages 535-542.
Crossref
Crossref
Siqing Fu, Jiashu Dong, Chunfang Wang & Guanming Chen. (2010) Parental attitudes toward genetic testing for prelingual deafness in China. International Journal of Pediatric Otorhinolaryngology 74:10, pages 1122-1125.
Crossref
Crossref
Yu-Fen GuoXiao-Wen LiuBai-Cheng XuYi-Ming ZhuYan-Li WangFei-Fan ZhaoDa-Yong WangYa-Li ZhaoYu-Bin JiQiu-Ju Wang. (2010) Analysis of a Large-Scale Screening of Mitochondrial DNA m.1555A>G Mutation in 2417 Deaf–Mute Students in Northwest of China. Genetic Testing and Molecular Biomarkers 14:4, pages 527-531.
Crossref
Crossref
Yu-Fen Guo, Yan-Li Wang, Bai-Cheng Xu, Xiao-Wen Liu, Yi-Ming Zhu, Fei-Fan Zhao, Yu-Bin Ji, Ying Zhou, Jian-Qiang Li, Qian Li, Da-Yong Wang & Qiu-ju Wang. (2010) Identification of two novel mutations, c.232T>C and c.2006A>T, in SLC26A4 in a Chinese family associated with enlarged vestibular aqueduct. International Journal of Pediatric Otorhinolaryngology 74:7, pages 831-835.
Crossref
Crossref
Akin Yilmaz, Sevda Menevse, Yildirim Bayazit, Recep Karamert, Volkan Ergin & Adnan Menevse. (2009) Two Novel Missense Mutations in the Connexin 26 Gene in Turkish Patients with Nonsyndromic Hearing Loss. Biochemical Genetics 48:3-4, pages 248-256.
Crossref
Crossref
Byung Yoon ChoiAndrew K. StewartKatherine K. NishimuraWon Jae ChaMoon-Woo SeongSung Sup ParkSeung Won KimYang Sook ChunJong Woo ChungShi-Nae ParkSun O. ChangChong-Sun KimSeth L. AlperAndrew J. GriffithSeung-Ha Oh. (2009) Efficient Molecular Genetic Diagnosis of Enlarged Vestibular Aqueducts in East Asians. Genetic Testing and Molecular Biomarkers 13:5, pages 679-687.
Crossref
Crossref
Pu Dai, Andrew K. Stewart, Fouad Chebib, Ann Hsu, Julia Rozenfeld, Deliang Huang, Dongyang Kang, Va Lip, Hong Fang, Hong Shao, Xin Liu, Fei Yu, Huijun Yuan, Margaret Kenna, David T. Miller, Yiping Shen, Weiyan Yang, Israel Zelikovic, Orah S. Platt, Dongyi Han, Seth L. Alper & Bai-Lin Wu. (2009)
Distinct and novel
SLC26A4/Pendrin
mutations in Chinese and U.S. patients with nonsyndromic hearing loss
. Physiological Genomics 38:3, pages 281-290.
Crossref
Crossref
Saima Anwar, Saima Riazuddin, Zubair M Ahmed, Saba Tasneem, Ateeq-ul-Jaleel, Shahid Y Khan, Andrew J Griffith, Thomas B Friedman & Sheikh Riazuddin. (2009) SLC26A4 mutation spectrum associated with DFNB4 deafness and Pendred's syndrome in Pakistanis. Journal of Human Genetics 54:5, pages 266-270.
Crossref
Crossref
Annelies Konings, Guy Van Camp, Alain Goethals, Els Van Eyken, Ann Vandevelde, Jamila Ben Azza, Nils Peeters, Wim Wuyts, Hubert Smeets & Lut Van Laer. (2008) Mutation analysis of mitochondrial DNA 12SrRNA and tRNASer(UCN) genes in non-syndromic hearing loss patients. Mitochondrion 8:5-6, pages 377-382.
Crossref
Crossref