Recurrent mutations in the deafness gene GJB2 (connexin 26) in British Asian families.

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Bibliographic Details
Title: Recurrent mutations in the deafness gene GJB2 (connexin 26) in British Asian families.
Authors: Rickard S, Kelsell DP, Sirimana T, Rajput K, MacArdle B, Bitner-Glindzicz M
Source: Journal of medical genetics [J Med Genet] 2001 Aug; Vol. 38 (8), pp. 530-3.
Publication Type: Letter; Research Support, Non-U.S. Gov't
Journal Info: Publisher: British Medical Association Country of Publication: England NLM ID: 2985087R Publication Model: Print Cited Medium: Internet ISSN: 1468-6244 (Electronic) Linking ISSN: 00222593 NLM ISO Abbreviation: J Med Genet Subsets: MEDLINE
Database: MEDLINE Ultimate
Description
ISSN:1468-6244
DOI:10.1136/jmg.38.8.530