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DFNB89, a novel autosomal recessive nonsyndromic hearing impairment locus on chromosome 16q21-q23.2

DFNB89 is a novel autosomal recessive non-syndromic hearing impairment (ARNSHI) locus that was mapped to 16q21-q23.2. Linkage to the region was established by carrying out genome-wide linkage scans in two unrelated, consanguineous Pakistani families segregating ARNSHI. The maximum multipoint LOD sco...

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Autors principals: Basit, Sulman, Lee, Kwanghyuk, Habib, Rabia, Chen, Leon, Umm-e-Kalsoom, Santos-Cortez, Regie Lyn P., Azeem, Zahid, Andrade, Paula, Ansar, Muhammad, Ahmad, Wasim, Leal, Suzanne M.
Format: Artigo
Idioma:Inglês
Publicat: 2010
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Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC3312604/
https://ncbi.nlm.nih.gov/pubmed/21181198
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00439-010-0934-0
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