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Fetal and Pediatric Pathology Volume 39, 2020 - Issue 1
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Articles

Role of GJB2 and GJB6 in Iranian Nonsyndromic Hearing Impairment: From Molecular Analysis to Literature Reviews

Masoumeh FalahENT and Head & Neck Research Center and Department, The Five Senses Institute, Hazrat Rasool Akram Hospital, Iran University of Medical Sciences, Tehran, Islamic Republic of Iran; View further author information
,
Massoud HoushmandENT and Head & Neck Research Center and Department, The Five Senses Institute, Hazrat Rasool Akram Hospital, Iran University of Medical Sciences, Tehran, Islamic Republic of Iran; ;Department of Medical Genetics, National Institute for Genetic Engineering and Biotechnology, Tehran, Islamic Republic of Iran; Correspondence[email protected]
View further author information
,
Maryam BalaliENT and Head & Neck Research Center and Department, The Five Senses Institute, Hazrat Rasool Akram Hospital, Iran University of Medical Sciences, Tehran, Islamic Republic of Iran; View further author information
,
Alimohamad AsghariSkull Base Research Center, Iran University of Medical Sciences, Tehran, Islamic Republic of IranView further author information
,
Zohreh BagherENT and Head & Neck Research Center and Department, The Five Senses Institute, Hazrat Rasool Akram Hospital, Iran University of Medical Sciences, Tehran, Islamic Republic of Iran; View further author information
,
Rafieh AlizadehENT and Head & Neck Research Center and Department, The Five Senses Institute, Hazrat Rasool Akram Hospital, Iran University of Medical Sciences, Tehran, Islamic Republic of Iran; View further author information
&
Mohammad FarhadiENT and Head & Neck Research Center and Department, The Five Senses Institute, Hazrat Rasool Akram Hospital, Iran University of Medical Sciences, Tehran, Islamic Republic of Iran; Correspondence[email protected]
View further author information
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Pages 1-12 | Received 10 Apr 2019, Accepted 20 May 2019, Published online: 19 Jun 2019

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Mahsa Farjami, Mozhgan Fathi, Mohammad Mehdi Ghasemi, Mohsen Rajati, Atieh Eslahi, Malihe Alimardani & Majid Mojarrad. (2021) Investigation of MYO15A and MYO7A Mutations in Iranian Patients with Nonsyndromic Hearing Loss. Fetal and Pediatric Pathology 40:2, pages 121-130.
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Articles from other publishers (11)

Ahmad Daneshi, Masoud Garshasbi, Mohammad Farhadi, Khalil Ghasemi Falavarjani, Mohammad Vafaee-Shahi, Navid Almadani, MohammadSina Zabihi, Mohammad Amin Ghalavand & Masoumeh Falah. (2023) Genetic insights into PHARC syndrome: identification of a novel frameshift mutation in ABHD12. BMC Medical Genomics 16:1.
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Sima Rayat, Mohammad Farhadi, Hessamaldin Emamdjomeh, Saeid Morovvati & Masoumeh Falah. (2022) Analysis of TMIE gene mutations including the first large deletion of exon 1 with autosomal recessive non-syndromic deafness. BMC Medical Genomics 15:1.
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Neslihan Duzkale, Gamze Tas Aygar, Kemal Keseroglu, Murad Mutlu & Mehmet Birol Ugur. (2022) Causal Variants of the GJB6 Gene are Associated with Hearing Loss and Skin Manifestations: A Case Report from Turkey. International Journal of Dermatology and Venereology 5:3, pages 166-168.
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Mohammad Vafaee-Shahi, Mohammad Farhadi, Ehsan Razmara, Saeid Morovvati, Saeide Ghasemi, Seyedeh Sedigheh Abedini, Zohreh Bagher, Rafieh Alizadeh & Masoumeh Falah. (2021) Novel phenotype and genotype spectrum of NARS2 and literature review of previous mutations. Irish Journal of Medical Science (1971 -) 191:4, pages 1877-1890.
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Mojgan Babanejad, Maryam Beheshtian, Fereshteh Jamshidi, Marzieh Mohseni, Kevin T. Booth, Kimia Kahrizi & Hossein Najmabadi. (2022) Genetic etiology of hearing loss in Iran. Human Genetics 141:3-4, pages 623-631.
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Maryam Jalessi, Mohammad Saeed Gholami, Ehsan Razmara, Sajad Hassanzadeh, Alireza Sadeghipour, Amin Jahanbakhshi, Alireza Tabibkhooei, Eshagh Bahrami & Masoumeh Falah. (2021) Association between TBXT rs2305089 polymorphism and chordoma in Iranian patients identified by a developed T‐ARMS‐PCR assay . Journal of Clinical Laboratory Analysis 36:1.
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Ehsan Abbaspour Rodbaneh, Mohammad Panahi, Bahareh Rahimi, Haleh Mokabber, Reza Farajollahi & Behzad Davarnia. (2021) GJB2 mutations in Iranian Azeri population with autosomal recessive nonsyndromic hearing loss (ARNSHL): First report of c.238 C>A mutation in Iran. Journal of Clinical Laboratory Analysis 35:11.
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Wasiu Lanre Adeyemo, Olutayo James, Babatunde A. Bamigboye, Moronke D. Akinola, Olawale O. Adamson, Benjamin N. Nkemjika, Adebayo A. Ibikunle, Mobolanle O. Ogunlewe, Akinola L. Ladeinde & Azeez Butali. (2021) Missense Variants Within GJB2 Gene Locus and the Risk of Hearing Defects in Nonsyndromic Cleft Lip and Palate. Journal of Craniofacial Surgery 32:7, pages e676-e678.
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Mohammad Farhadi, Ehsan Razmara, Maryam Balali, Yeganeh Hajabbas Farshchi & Masoumeh Falah. (2021) How Transmembrane Inner Ear (TMIE) plays role in the auditory system: A mystery to us. Journal of Cellular and Molecular Medicine 25:13, pages 5869-5883.
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Hongyang Wang, Yun Gao, Jing Guan, Lan Lan, Ju Yang, Wenping Xiong, Cui Zhao, Linyi Xie, Lan Yu, Dayong Wang & Qiuju Wang. (2021) Phenotypic Heterogeneity of Post-lingual and/or Milder Hearing Loss for the Patients With the GJB2 c.235delC Homozygous Mutation. Frontiers in Cell and Developmental Biology 9.
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Mahbobeh Koohiyan, Farideh Koohian & Fatemeh Azadegan‐Dehkordi. (2019) GJB2 ‐related hearing loss in central Iran: Review of the spectrum and frequency of gene mutations . Annals of Human Genetics 84:2, pages 107-113.
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