Screening of Myo7A Mutations in Iranian Patients with Autosomal Recessive Hearing Loss from West of Iran

• Główni autorzy: Samira ASGHARZADE (Autor), Somayeh REIISI (Autor), Mohammad Amin TABATABAIEFAR (Autor), Morteza HASHEMZADEH CHALESHTORI (Autor)
• Format: Książka
• Wydane: Tehran University of Medical Sciences, 2017-01-01T00:00:00Z.
• Hasła przedmiotowe: article
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Background: Hearing loss (HL) is the most frequent neurosensory impairment. HL is highly heterogeneous defect. This disorder affects 1 out of 500 newborns. This study aimed to determine the role of DFNB2 locus and frequency of MYO7A gene mutations in a population from west of Iran. Methods: Thirty f...