An Extended Iranian Family with Autosomal Dominant Non-syndromic Hearing Loss Associated with A Nonsense Mutation in the DIAPH1 Gene

Marzieh Mohseni ¹ , Yusuf Mohammadi ¹ , Farzane Zare Ashrafi ¹, Fatemeh Ghodratpour ¹, Khadijeh Jalalvand ¹, Sanaz Arzhangi ¹, Mojgan Babanejad ¹, Mohammad Hossein Azizi ², Kimia Kahrizi ¹, Hossein Najmabadi ¹ *

Cited by CrossRef: 2

1- Li S, Li S, Chen D, Zhao S, Liu C, Zhang R, Chen Y, Guo X, Song X. Case report of a novel mutation in the TNC gene in Chinese patients with nonsyndromic hearing loss. 2024;103(16):e37702 [Crossref]

2- Feng Q, Jiang L, Zhang S, He C, Mei L, Liu Y. A novel frameshift mutation in the DIAPH1 gene causes a Chinese family autosomal dominant nonsyndromic hearing loss. Gene. 2025;936:149088 [Crossref]

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A Monthly Peer-Reviewed Medical Journal Published by the Academy of Medical Sciences of the I.R. Iran; Indexed in PubMed/MEDLINE, ISI Web of Science, EMBASE, SCOPUS, CINHAL, PASCAL, CSA, SID, ISSN: Print 1029-2977, Online 1735-3947.The impact factor of Archives of Iranian Medicine according to Journal Citation Reports® (JCR®) 2016 is 1.20.