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- Title
[Connexin 26 mutation and keratitis-ichthyosis-deafness (KID) syndrome].
- Authors
Binder, Barbara; Hennies, Hans Christian; Kraschl, Raimund; Smolle, Josef
- Abstract
Keratitis-ichthyosis-deafness syndrome (KID syndrome) is an extremely rare disorder. Inheritance is autosomal dominant but many cases occur sporadically following a spontaneous mutation. The cause of KID syndrome are missense mutations of the gene GJB2, encoding connexin 26.
- Publication
Journal der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG, 2005, Vol 3, Issue 2, p105
- ISSN
1610-0379
- Publication type
Journal Article
- DOI
10.1111/j.1610-0378.2005.04748.x