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