论文信息 - Novel mutations in the pejvakin gene are associated with autosomal recessive non‐syndromic hearing loss in Iranian families - 字舞流文

Novel mutations in the pejvakin gene are associated with autosomal recessive non‐syndromic hearing loss in Iranian families

M. Dolati | E. Farrokhi | M. Hashemzadeh Chaleshtori | A. Crosby | L. Hoghooghi Rad | M. Simpson | S. Amani Geshnigani