Logo-aim
Arch Iran Med. 2024;27(4): 223-226. doi: 10.34172/aim.2024.32
PMID: 38685849        PMCID: PMC11097304

Case Report

Identification of a Novel Homozygous Mutation in PRDM12 Gene in a Patient with Hereditary Sensory and Autonomic Neuropathy Type VIII

Amir Hossein Ebrahimi 1,2 ORCID, Manzar Bolhassani 1 ORCID, Mohammad Reza Zarei 3 ORCID, Matin Heidari 1,2 ORCID, Amin ArdeshirDavani 4, Amir Hosein Mehrtash 4, Zahra Shiri 1 ORCID, Masoud Heidari 1 ORCID, Morteza Soleyman-Nejad 1, Mohammad Hossein Taskhiri 1, Arefeh Norouzbeigi 1, Mansour Heidari 1,5 * ORCID

Cited by CrossRef: 0


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.