Genetic Linkage Analysis of 15 DFNB Loci in a Group of Iranian Families with Autosomal Recessive Hearing Loss

BACKGROUND: Hearing loss (HL) is the most frequent sensory birth defect in humans. Autosomal recessive non-syndromic HL (ARNSHL) is the most common type of hereditary HL. It is extremely heterogeneous and over 70 loci (known as DFNB) have been identified. This study was launched to determine the rel...

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Main Authors: Tabatabaiefar, MA, Alasti, F, Zohour, M Montazer, Shariati, L, Farrokhi, E, Farhud, DD, Camp, GV, Noori-Daloii, MR, Chaleshtori, M Hashemzadeh
Format: Artigo
Language:Inglês
Published: Tehran University of Medical Sciences 2011
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Original Article
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC3481767/
https://ncbi.nlm.nih.gov/pubmed/23113071
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