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 |
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Jazyk: | angličtina |
Zdroj: | Journal of medical genetics [J Med Genet] 2003 May; Vol. 40 (5), pp. e68. |
DOI: | 10.1136/jmg.40.5.e68 |
Databáze: | MEDLINE |
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