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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Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Prif Awduron: 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
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: Public Library of Science 2014
Pynciau:
Research Article
Mynediad Ar-lein: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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