Role of DFNB1 mutations in hereditary hearing loss among assortative mating hearing impaired families from South India

Por Amritkumar, Pavithra, Jeffrey, Justin Margret, Chandru, Jayasankaran, Vanniya S, Paridhy, Kalaimathi, M., Ramakrishnan, Rajagopalan, Karthikeyen, N. P., Srikumari Srisailapathy, C. R.
Publicado no BMC Med Genet (2018)

Functional consequences of novel connexin 26 mutations associated with hereditary hearing loss

Por Mani, Ram Shankar, Ganapathy, Aparna, Jalvi, Rajeev, Srikumari Srisailapathy, C R, Malhotra, Vikas, Chadha, Shelly, Agarwal, Arun, Ramesh, Arabandi, Rangasayee, Raghunath Rao, Anand, Anuranjan
Publicado em 2009