DOI:
10.1055/s-00029027
Journal of Pediatric Genetics
LinksClose Window
References
Bhalla S, Sharma R, Khandelwal G, Panda NK, Khullar M.
Low incidence of GJB2, GJB6 and mitochondrial DNA mutations in North Indian patients with non-syndromic hearing impairment.
Biochem Biophys Res Commun 2009;
385 (03) 445-448
We do not assume any responsibility for the contents of the web pages of other providers.