Haplotype Analysis of Seven Non-Syndromeic Autosomal Recessive Hearing Loss Loci in Iranian Families

Objective: Hearing impairment is the most frequent sensorineural defect in 2 forms, syndromic and non-syndromic. The aim of this study is haplotype analysis of seven loci of non-syndromic autosomal recessive hearing loss in Iranian families. Materials & Methods: In this descriptive study, forty...

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Main Authors: Ramak Badr (Author), Bahareh Shoja-Saffar (Author), Niloofar Bazzaz-Zadegan (Author), Khadijeh Jalalvand (Author), Kimia Kahrizi (Author), Hossein Najm-Abadi (Author)
Format: Book
Published: University of Social Welfare and Rehabilitation Sciences, 2010-01-01T00:00:00Z.
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