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Localization of a novel autosomal recessive nonsyndromic hearing impairment locus DFNB65 to chromosome 20q13.2–q13.32

Abstract Autosomal recessive nonsyndromic hearing impairment (ARNSHI) is the most frequent form of prelingual hereditary hearing loss in humans. Between 75 and 80% of all nonsyndromic deafness is inherited in an autosomal recessive pattern. Using linkage analysis, we have mapped a novel gene respons...

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Detalhes bibliográficos
Main Authors: Tariq, Aamira, Santos, Regie Lyn P., Khan, Mohammad Nasim, Lee, Kwanghyuk, Hassan, Muhammad Jawad, Ahmad, Wasim, Leal, Suzanne M.
Formato: Artigo
Idioma:Inglês
Publicado em: 2006
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2909102/
https://ncbi.nlm.nih.gov/pubmed/16596430
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00109-005-0023-3
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