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pro vyhledávání: '"Saeid Mahmodian"'
Autor:
Masoumeh Falah, Massoud Houshmand, Susan Akbaroghli, Saeid Mahmodian, Yaser Ghavami, Mohammad Farhadi
Publikováno v:
Iranian Journal of Basic Medical Sciences, Vol 14, Iss 50 (2011)
AbstractObjective(s)Despite the enormous heterogeneity of genetic hearing loss, most non-syndromic hearing losses are caused by mutations in the GJB2 gene. We aimed to characterize the mutation profiles of 100 Iranian deaf patients that were under 10
Externí odkaz:
https://doaj.org/article/946f42ea073144c891b6abdd19631e87
