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

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...

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Vydáno v:Iran J Public Health
Hlavní autoři: ASGHARZADE, Samira, REIISI, Somayeh, TABATABAIEFAR, Mohammad Amin, CHALESHTORI, Morteza HASHEMZADEH
Médium: Artigo
Jazyk:Inglês
Vydáno: Tehran University of Medical Sciences 2017
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Original Article
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC5401939/
https://ncbi.nlm.nih.gov/pubmed/28451532
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