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

RamShankar, M. ; Girirajan, S. ; Dagan, O. ; Ravi Shankar, H. M. ; Jalvi, R. ; Rangasayee, R. ; Avraham, K. B. ; Anand, A. (2003) Contribution of connexin26 (GJB2) mutations and founder effect to non-syndromic hearing loss in India Journal of Medical Genetics, 40 (5). e68_1-e68_6. ISSN 0022-2593

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Official URL: http://jmg.bmj.com/content/40/5/e68.short

Related URL: http://dx.doi.org/10.1136/jmg.40.5.e68

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Item Type:Article
Source:Copyright of this article belongs to BMJ Publishing Group.
ID Code:66426
Deposited On:24 Oct 2011 08:50
Last Modified:18 May 2016 13:58

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