Keywords = MYO15A
Number of Articles: 2
1. The worldwide frequency of MYO15A gene mutations in patients with autosomal recessive non-syndromic hearing loss: A meta‐analysis

Volume 23, Issue 7, July 2020, Pages 841-848

Mahsa Farjami; Reza Asadi; Fahimeh Afzal Javan; Malihe Alimardani; Saeed Eslami; Sima Mansoori Derakhshan; Atieh Eslahi; Majid Mojarad

2. Screening of DFNB3 in Iranian families with autosomal recessive non-syndromic hearing loss reveals a novel pathogenic mutation in the MyTh4 domain of the MYO15A gene in a linked family

Volume 19, Issue 7, July 2016, Pages 772-778

Somayeh Reiisi; Mohammad Amin Tabatabaiefar; Mohammad Hosein Sanati; Morteza Hashemzadeh Chaleshtori

Iranian Journal of Basic Medical Sciences

Journal Archive