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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...

詳細記述

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書誌詳細
主要な著者: Tabatabaiefar, MA, Alasti, F, Zohour, M Montazer, Shariati, L, Farrokhi, E, Farhud, DD, Camp, GV, Noori-Daloii, MR, Chaleshtori, M Hashemzadeh
フォーマット: Artigo
言語:Inglês
出版事項: Tehran University of Medical Sciences 2011
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC3481767/
https://ncbi.nlm.nih.gov/pubmed/23113071
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