1. A Village in the Southeastern Region of Iran Harboring the c.716T>A (p.Val239Asp) Mutation in SLC26A4

Farzane Zare Ashrafi , Saeed Dorgaleleh, Raziye Rezvani Rezvandeh, Negar Kazemi, Nasrin Azizi, Masoud Edizadeh, Mohammad Hossein Azizi, Kimia Kahrizi, Hossein Najmabadi, Reza Najafipour, Marzieh Mohseni*

Arch Iran Med. 2024;27(9): 522-526. doi: 10.34172/aim.28745

PMCID: PMC11496598 PMID: 39465527 Scopus ID: 85206813812

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Case Report

2. A Novel Candidate Gene MACF1 is Associated with Autosomal Dominant Non-syndromic Hearing Loss in an Iranian Family

Niloofar Bazazzadegan* , Mojgan Babanejad , Susan Banihashemi, Sanaz Arzhangi, Kimia Kahrizi , Kevin TA Booth , Hossein Najmabadi

Arch Iran Med. 2025;28(1): 63-66. doi: 10.34172/aim.31746

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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.