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DFNB44, a Novel Autosomal Recessive Non-Syndromic Hearing Impairment Locus, Maps to Chromosome 7p14.1-q11.22

The genetic etiology for many forms of hearing impairment (HI) is very diverse. Non-syndromic HI (NSHI) is one of the most heterogeneous traits known. Autosomal recessive forms of prelingual HI account for ∼75% of hereditary cases. A novel autosomal recessive NSHI locus, DFNB44, was mapped to a 20.9...

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Detalhes bibliográficos
Main Authors: Ansar, Muhammad, Chahrour, Maria H., ud Din, Mohammad Amin, Arshad, Muhammad, Haque, Sayedul, Pham, Thanh L., Yan, Kai, Ahmad, Wasim, Leal, Suzanne M.
Formato: Artigo
Idioma:Inglês
Publicado em: 2004
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2920138/
https://ncbi.nlm.nih.gov/pubmed/15583425
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1159/000081446
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