Molecular screening of deafness in Algeria: High genetic heterogeneity involving DFNB1 and the Usher loci, DFNB2/USH1B, DFNB12/USH1D and DFNB23/USH1F-Reference-Cited by-同舟云学术

Molecular screening of deafness in Algeria: High genetic heterogeneity involving DFNB1 and the Usher loci, DFNB2/USH1B, DFNB12/USH1D and DFNB23/USH1F

Published:2009-07 Issue:4 Volume:52 Page:174-179
ISSN:1769-7212
Container-title:European Journal of Medical Genetics
language:en
Short-container-title:European Journal of Medical Genetics

Author:

Ammar-Khodja Fatima,Faugère Valérie,Baux David,Giannesini Claire,Léonard Susana,Makrelouf Mohamed,Malek Rahia,Djennaoui Djamel,Zenati Akila,Claustres Mireille,Roux Anne-Françoise

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics,General Medicine

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3. Connexin26 mutations associated with the most common form of non-syndromic neurosensory autosomal recessive deafness (DFNB1) in Mediterraneans;Zelante;Hum. Mol. Genet.,1997

4. Connexin-26 mutations in sporadic and inherited sensorineural deafness;Estivill;Lancet,1998

5. Molecular epidemiology of DFNB1 deafness in France;Roux;BMC Med. Genet.,2004

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