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Arch Iran Med. 2023;26(3): 176-180. doi: 10.34172/aim.2023.27
PMID: 37543941        PMCID: PMC10685723

Case Report

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

Marzieh Mohseni 1 ORCID, Yusuf Mohammadi 1 ORCID, 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 * ORCID

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]
3- Kurasawa S, Ganaha A, Ayabe S, Yoshiki A, Kawama F, Kitayama S, Tabuchi K, Yamashita K, Ueyama T. Hearing loss occurs prior to thrombocytopenia in both mice and humans with DFNA1. The FASEB Journal. 2025;39(2) [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.