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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Detalles Bibliográficos
Autores principales: 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: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3885616/
https://www.ncbi.nlm.nih.gov/pubmed/24416283
http://dx.doi.org/10.1371/journal.pone.0084773

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3885616/
https://www.ncbi.nlm.nih.gov/pubmed/24416283
http://dx.doi.org/10.1371/journal.pone.0084773

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