Novel mutations in the pejvakin gene are associated with autosomal recessive non-syndromic hearing loss in Iranian families期刊界 All Journals 搜尽天下杂志传播学术成果专业期刊搜索期刊信息化学术搜索

Novel mutations in the pejvakin gene are associated with autosomal recessive non-syndromic hearing loss in Iranian families

Authors:	Hashemzadeh Chaleshtori M Simpson M A Farrokhi E Dolati M Hoghooghi Rad L Amani Geshnigani S Crosby A H

Affiliation:	Cellular and Molecular Research Center, Shahrekord University of Medical Sciences, Shahrekord, Iran;, Department of Medical Genetics, St George's Hospital Medical School, University of London, Cranmer Terrace, London, UK;, and Department of Biochemistry and Genetics, School of Medicine, Qom University of Medical Sciences, Qom, Iran

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