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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: 1

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]

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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.