A novel autosomal recessive non-syndromic hearing impairment locus (DFNB47) maps to chromosome 2p25.1-p24.3

Hereditary hearing impairment (HI) displays extensive genetic heterogeneity. Autosomal recessive (AR) forms of prelingual HI account for ~75% of cases with a genetic etiology. A novel AR non-syndromic HI locus (DFNB47) was mapped to chromosome 2p25.1-p24.3, in two distantly related Pakistani kindred...

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Main Authors: Hassan, Muhammad Jawad, Santos, Regie Lyn P., Rafiq, Muhammad Arshad, Chahrour, Maria H., Pham, Thanh L., Wajid, Muhammad, Hijab, Nadine, Wambangco, Michael, Lee, Kwanghyuk, Ansar, Muhammad, Yan, Kai, Ahmad, Wasim, Leal, Suzanne M.
Formato: Artigo
Idioma:Inglês
Publicado em: 2005
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2909103/
https://ncbi.nlm.nih.gov/pubmed/16261342
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00439-005-0079-8
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