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
Citation
S. Rickard et al., Recurrent mutations in the deafness gene GJB2 (connexin 26) in British Asian families, J MED GENET, 38(8), 2001, pp. 530-533
Citations number
20
Categorie Soggetti
Research/Laboratory Medicine & Medical Tecnology","Molecular Biology & Genetics
Journal title
JOURNAL OF MEDICAL GENETICS
ISSN journal
00222593 → ACNP
Volume
38
Issue
8
Year of publication
2001
Pages
530 - 533
Database
ISI
SICI code
0022-2593(200108)38:8<530:RMITDG>2.0.ZU;2-M