We found a match
Your institution may have access to this item. Find your institution then sign in to continue.
- Title
A large deletion including most of GJB6 in recessive non syndromic deafness: a digenic effect?
- Authors
Pallares-Ruiz, Nathalie; Blanchet, Patricia; Mondain, Michel; Claustres, Mireille; Roux, Anne-Francoise
- Abstract
Congenital profound deafness has a known genetic origin in more than 50% of all cases. The majority of the non syndromic hearing loss (NSHL) show an autosomal recessive inheritance. Mutations in the GJB2 gene (connexin 26) account for more than 50% of the recessive non syndromic deafness (DFNB1) among 30 loci. Other connexin genes have been more rarely involved and attention was given here to the GJB6 gene (connexin 30). We show that homozygous deletion of a minimal 150 kb region encompassing this gene causes NSHL. More strikingly, association of this deletion in trans of the GJB2 gene 35delG or E47X mutations is also associated with NSHL.
- Publication
European journal of human genetics : EJHG, 2002, Vol 10, Issue 1, p72
- ISSN
1018-4813
- Publication type
Journal Article
- DOI
10.1038/sj.ejhg.5200762