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

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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.