Logo-aim
Arch Iran Med. 2025;28(1): 63-66. doi: 10.34172/aim.31746
PMID: 40001331        PMCID: PMC11862395

Case Report

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

Niloofar Bazazzadegan 1 * ORCID, Mojgan Babanejad 1 ORCID, Susan Banihashemi 1, Sanaz Arzhangi 1, Kimia Kahrizi 1 ORCID, Kevin TA Booth 2,3 ORCID, Hossein Najmabadi 1 ORCID

Cited by CrossRef:

1- Xi J, Deng F, Liang M, Ding Y, Li X, Gu Z, Lin Z, Liu Z, Li X. Global developmental delay and focal seizures in individuals with de novo truncating MACF1 variants. Hum Genomics. 2026;20(1) [Crossref]

SCImago Journal & Country Rank

About Us

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.