Article info
Online mutation report
Contribution of connexin26 (GJB2) mutations and founder effect to non-syndromic hearing loss in India
- Correspondence to: Dr A Anand, Molecular Biology and Genetics Unit, Jawaharlal Nehru Centre for Advanced Scientific Research, Bangalore 560 064, India; anand{at}jncasr.ac.in
Citation
Contribution of connexin26 (GJB2) mutations and founder effect to non-syndromic hearing loss in India
Publication history
- First published May 1, 2003.
Online issue publication
May 01, 2003
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Copyright 2003 Journal of Medical Genetics