Screening of 10 DFNB Loci Causing Autosomal Recessive Non-Syndromic Hearing Loss in Two Iranian Populations Negative for GJB2 Mutations

• Κύριοι συγγραφείς: Mahbobeh KOOHIYAN (Συγγραφέας), Somayeh REIISI (Συγγραφέας), Fatemeh AZADEGAN-DEHKORDI (Συγγραφέας), Mansoor SALEHI (Συγγραφέας), Hamidreza ABTAHI (Συγγραφέας), Morteza HASHEMZADEH-CHALESHTORI (Συγγραφέας), Mohammad Reza NOORI-DALOII (Συγγραφέας), Mohammad Amin TABATABAIEFAR (Συγγραφέας)
• Μορφή: Βιβλίο
• Έκδοση: Tehran University of Medical Sciences, 2019-09-01T00:00:00Z.
• Θέματα: article
• Διαθέσιμο Online: Connect to this object online.

Background: Autosomal recessive non-syndromic hearing loss (ARNSHL), one of the global public health concerns, is marked by a high degree of genetic heterogeneity. The role of GJB2, as the most common cause of ARNSHL, is only <20% in the Iranian population. Here, we aimed to determine the relativ...