Molecular epidemiology of DFNB1 deafness in France-Reference-Cited by-同舟云学术

Molecular epidemiology of DFNB1 deafness in France

Published:2004-03-06 Issue:1 Volume:5 Page:
ISSN:1471-2350
Container-title:BMC Medical Genetics
language:en
Short-container-title:BMC Med Genet

Author:

Roux Anne-Françoise,Pallares-Ruiz Nathalie,Vielle Anne,Faugère Valérie,Templin Carine,Leprevost Dorothée,Artières Françoise,Lina Geneviève,Molinari Nicolas,Blanchet Patricia,Mondain Michel,Claustres Mireille

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1186/1471-2350-5-5.pdf

Reference48 articles.

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2. Marziano NK, Casalotti SO, Portelli AE, Becker DL, Forge A: Mutations in the gene for connexin 26 (GJB2) that cause hearing loss have a dominant negative effect on connexin 30. Hum Mol Genet. 2003, 12: 805-812. 10.1093/hmg/ddg076.

3. Steel KP, Kros CJ: A genetic approach to understanding auditory function. Nat Genet. 2001, 27: 143-149. 10.1038/84758.

4. Kenneson A, Van Naarden Braun K, Boyle C: GJB2 (connexin 26) variants and nonsyndromic sensorineural hearing loss: a HuGE review. Genet Med. 2002, 4: 258-274. 10.1097/00125817-200207000-00004.

5. Calvo J, Rabionet R, Gasparini P, X E: Connexins and deafness Homepage. [ http://www.crg.es/deafness ]

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