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Viviana Chinetti, Sandra Iossa, Gennaro Auletta, Virginia Corvino, Maria De Luca, Francesca De Falco, Pasquale Giannini, Giorgio Lilli, Rita Malesci, Pasquale Riccardi, Elio Marciano & Annamaria Franzè. (2011) Mutational analysis for GJB2, GJB6, and GJB3 genes in Campania within a universal neonatal hearing screening programme. International Journal of Audiology 50:12, pages 866-870.
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Ida Jensen Friis, Kirsten Aaberg & Bjarke Edholm. (2023) Causes of hearing loss and implantation age in a cohort of Danish pediatric cochlear implant recipients. International Journal of Pediatric Otorhinolaryngology 171, pages 111640.
Crossref
Crossref
Tatiana Markova, Natalia Alekseeva, Maria Lalayants, Oxana Ryzhkova, Olga Shatokhina, Nailya Galeeva, Elena Bliznetz, Oleg Belov, Svetlana Chibisova, Alexander Polyakov & George Tavartkiladze. (2022) Audiological Evidence of Frequent Hereditary Mild, Moderate and Moderate-to-Severe Hearing Loss. Journal of Personalized Medicine 12:11, pages 1843.
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Yue Qiu, Jianglin Zheng, Sen Chen & Yu Sun. (2022) Connexin Mutations and Hereditary Diseases. International Journal of Molecular Sciences 23:8, pages 4255.
Crossref
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Pey-Yu Chen, Yin-Hung Lin, Tien-Chen Liu, Yi-Hsin Lin, Li-Hui Tseng, Ting-Hua Yang, Pei-Lung Chen, Chen-Chi Wu & Chuan-Jen Hsu. (2020) Prediction Model for Audiological Outcomes in Patients With GJB2 Mutations. Ear & Hearing 41:1, pages 143-149.
Crossref
Crossref
Fabio Mammano. (2019) Inner Ear Connexin Channels: Roles in Development and Maintenance of Cochlear Function. Cold Spring Harbor Perspectives in Medicine 9:7, pages a033233.
Crossref
Crossref
Francisco J. del Castillo & Ignacio del Castillo. (2017) DFNB1 Non-syndromic Hearing Impairment: Diversity of Mutations and Associated Phenotypes. Frontiers in Molecular Neuroscience 10.
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Jeffrey C. Wingard & Hong-Bo Zhao. (2015) Cellular and Deafness Mechanisms Underlying Connexin Mutation-Induced Hearing Loss – A Common Hereditary Deafness. Frontiers in Cellular Neuroscience 9.
Crossref
Crossref
Y. Zhu, J. Chen, C. Liang, L. Zong, J. Chen, R.O. Jones & H.-B. Zhao. (2015) Connexin26 (GJB2) deficiency reduces active cochlear amplification leading to late-onset hearing loss. Neuroscience 284, pages 719-729.
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Haruo Yoshida, Haruo Takahashi, Yukihiko Kanda & Shin-ichi Usami. (2013) Long term speech perception after cochlear implant in pediatric patients with GJB2 mutations. Auris Nasus Larynx 40:5, pages 435-439.
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Diana P. Popova, Radka Kaneva, Sonya Varbanova & Todor M. Popov. (2011) Prevalence of GBJ2 mutations in patients with severe to profound congenital nonsyndromic sensorineural hearing loss in Bulgarian population. European Archives of Oto-Rhino-Laryngology 269:6, pages 1589-1592.
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Satoko Yoshikawa, Atsushi Kawano, Chieri Hayashi, Nobuhiro Nishiyama, Sachie Kawaguchi, Hiroko Furuse, Katsuhisa Ikeda, Mamoru Suzuki & Masahumi Nakagawa. (2011) The clinical features of patients with the homozygous 235delC and the compound-heterozygous Y136X/G45E of the GJB2 mutations (Connexin 26) in cochlear implant recipients. Auris Nasus Larynx 38:4, pages 444-449.
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Yan Ma, Tao Yang, Yun Li, Zheng Tao, Zhiwu Huang, Xiaohua Li, Yongchuan Chai, Zhiguo Ouyang, Xiaoming Shen & Hao Wu. (2010)
Genotype–phenotype correlation of two prevalent
GJB2
mutations in chinese newborn infants ascertained from the Universal Newborn Hearing Screening Program
. American Journal of Medical Genetics Part A 152A:11, pages 2912-2915.
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Jordan B. Hochman, Tracy L. Stockley, D. Shipp, Vincent Y. W. Lin, Joseph M. Chen & Julian M. Nedzelski. (2010) Prevalence of Connexin 26 (GJB2) and Pendred (SLC26A4) Mutations in a Population of Adult Cochlear Implant Candidates. Otology & Neurotology 31:6, pages 919-922.
Crossref
Crossref
Ivona SansovićJelena KneževićVesna MusaniPavel SeemanIngeborg BarišićJasminka Pavelić. (2009)
GJB2
Mutations in Patients with Nonsyndromic Hearing Loss from Croatia
. Genetic Testing and Molecular Biomarkers 13:5, pages 693-699.
Crossref
Crossref
Norihito Takeichi, Masaaki Kashiwamura, Yuji Nakamaru, Takashi Tsubuku, Satoshi Fukuda, Mika Suzuki & Shinichi Usami. (2009) Effective case of genetic testing in a bilateral deafness patient. AUDIOLOGY JAPAN 52:4, pages 214-219.
Crossref
Crossref
Charles M Bower & Patti F Martin. (2008) Infant hearing screening. Current Opinion in Otolaryngology & Head & Neck Surgery 16:6, pages 562-568.
Crossref
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Haris Kokotas, Maria Theodosiou, George Korres, Maria Grigoriadou, Elisabeth Ferekidou, Aglaia Giannoulia-Karantana, Michael B. Petersen & Stavros Korres. (2008) Sudden hearing loss in a family with GJB2 related progressive deafness. International Journal of Pediatric Otorhinolaryngology 72:11, pages 1735-1740.
Crossref
Crossref