论文信息 - The role and spectrum of SLC26A4 mutations in Iranian patients with autosomal recessive hereditary deafness - 字舞流文

The role and spectrum of SLC26A4 mutations in Iranian patients with autosomal recessive hereditary deafness

E. Farrokhi | N. Bagheri | M. Tabatabaiefar | Nasrin Yazdanpanahi | Mohammad Amin Tabatabaiefar | M. Hashemzadeh Chaleshtori | Fatemeh Azadegan Dehkordi | N. Yazdanpanahi