Author = Mahsa Farjami
PLA2G6 gene mutation and infantile neuroaxonal degeneration; report of three cases from Iran

Volume 24, Issue 9, September 2021, Pages 1190-1195

10.22038/ijbms.2021.55082.12340

Reza Jafarzadeh Esfehani; Atieh Eslahi; Mehran Beiraghi Toosi; Ariane Sadrnabavi; Mohammad Amin Kerachian; Mahsa Sadat Mohajeri Asl; Mahsa Farjami; Farzaneh Alizadeh; Majid Mojarad


The worldwide frequency of MYO15A gene mutations in patients with autosomal recessive non-syndromic hearing loss: A meta‚Äźanalysis

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

10.22038/ijbms.2020.35977.8563

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