Contribution of connexin26 (GJB2) mutations and founder effect to non-syndromic hearing loss in India.

Autor: RamShankar M; Molecular Biology and Genetics Unit, Jawaharlal Nehru Centre for Advanced Scientific Research, Bangalore, India., Girirajan S, Dagan O, Ravi Shankar HM, Jalvi R, Rangasayee R, Avraham KB, Anand A

Publikováno v: Journal of medical genetics [J Med Genet] 2003 May; Vol. 40 (5), pp. e68.