Mutations in GJB2 as Major Causes of Autosomal Recessive Non-Syndromic Hearing Loss: First Report of c.299-300delAT Mutation in Kurdish Population of Iran

por Azadegan-Dehkordi, Fatemeh, Bahrami, Tayyebe, Shirzad, Maryam, Karbasi, Gelareh, Yazdanpanahi, Nasrin, Farrokhi, Effat, Koohiyan, Mahbobeh, Tabatabaiefar, Mohammad Amin, Hashemzadeh-Chaleshtori, Morteza
Publicado 2019