Molecular Pathology of 6 Novel GJB2 Allelic Variants Detected in Familial and Sporadic Iranian Non Syndromic Hearing Loss Cases

Iranian Journal of Public Health

KGhatreh Samani¹  HPour Jafari²  DDFarhud³  KSafa Chaleshtori⁴  MKasiri⁵  MHashemzadeh Chaleshtori⁶  GRMobini⁷  DModarresinia⁷  EFarrokhi⁷  MShahrani⁷  MMansouri⁷  MJafari⁷  AHCrosby⁸ 

[1] Dept. of Clinical Chemistry, Tabriz University of Medical Sciences, Tabriz, Iran;Dept. of Genetics, School of Medicine, Hamadan University of Medical Sciences, Hamadan, Iran;Genetic Clinic, Valie Asr Sq., 16 Keshavarz Blvd., Tehran, Iran;Shahrekord Adminstration of Education and Training, Shahrekord, Iran;Welfare Organization of Chaharmahal va Bakhtiari, Shahrekord, Iran;1Cellular and Molecular Research Center, Shahrekord University of Medical Sciences, Shahrekord, Iran;Cellular and Molecular Research Center, Shahrekord University of Medical Sciences, Shahrekord, Iran;Dept. of Medical Genetics, St Georges Hospital Medical School, University of London, London, UK;

关键词: Deafness;    Connexin 26;    GJB2 gene;    Iran;   

DOI  :  

来源: DOAJ

【 授权许可】

Unknown