Localization of a novel autosomal recessive non-syndromic hearing impairment locus DFNB55 to chromosome 4q12-q13.2

Hereditary hearing impairment (HI) is the most genetically heterogeneous trait known in humans. So far, 54 autosomal recessive non-syndromic hearing impairment (ARNSHI) loci have been mapped, and 21 ARNSHI genes have been identified. Here is reported the mapping of a novel ARNSHI locus, DFNB55, to c...

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Main Authors: Irshad, S, Santos, RLP, Muhammad, D, Lee, K, McArthur, N, Haque, S, Ahmad, W, Leal, SM
Format: Artigo
Language:Inglês
Published: 2005
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Article
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC2910366/
https://ncbi.nlm.nih.gov/pubmed/16098016
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1399-0004.2005.00492.x
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