Non-Syndromic Hearing Impairment in India: High Allelic Heterogeneity among Mutations in TMPRSS3, TMC1, USHIC, CDH23 and TMIE

Mutations in the autosomal genes TMPRSS3, TMC1, USHIC, CDH23 and TMIE are known to cause hereditary hearing loss. To study the contribution of these genes to autosomal recessive, non-syndromic hearing loss (ARNSHL) in India, we examined 374 families with the disorder to identify potential mutations....

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Detalhes bibliográficos
Main Authors: Ganapathy, Aparna, Pandey, Nishtha, Srisailapathy, C. R. Srikumari, Jalvi, Rajeev, Malhotra, Vikas, Venkatappa, Mohan, Chatterjee, Arunima, Sharma, Meenakshi, Santhanam, Rekha, Chadha, Shelly, Ramesh, Arabandi, Agarwal, Arun K., Rangasayee, Raghunath R., Anand, Anuranjan
Formato: Artigo
Idioma:Inglês
Publicado em: Public Library of Science 2014
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3885616/
https://ncbi.nlm.nih.gov/pubmed/24416283
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0084773
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