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DFNB39, a recessive form of sensorineural hearing impairment, maps to chromosome 7q11.22–q21.12

This article describes the identification of a novel locus (DFNB39) responsible for an autosomal recessive form of hearing loss segregating in a Pakistani consanguineous family. The hearing impaired members of this family present with profound prelingual sensorineural hearing impairment and use sign...

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Detalhes bibliográficos
Main Authors: Wajid, Muhammad, Abbasi, Amir Ali, Ansar, Muhammad, Pham, Thanh L, Yan, Kai, Haque, Sayedul, Ahmad, Wasim, Leal, Suzanne M
Formato: Artigo
Idioma:Inglês
Publicado em: 2003
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2909101/
https://ncbi.nlm.nih.gov/pubmed/14512973
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/sj.ejhg.5201041
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