Connexin mutations in hearing loss, dermatological and neurological disorders
Author:
Publisher
Elsevier BV
Subject
Molecular Biology,Molecular Medicine
Reference80 articles.
1. Connexin mutations in X-linked Charcot-Marie-Tooth disease;Bergoffen;Science,1993
2. Mutations in the human connexin gene GJB3 cause erythrokeratodermia variabilis;Richard;Nat. Genet.,1998
3. Mutations in GJB6 cause hidrotic ectodermal dysplasia;Lamartine;Nat. Genet.,2000
4. Mutation in the gene for connexin 30.3 in a family with erythrokeratodermia variabilis;Macari;Am. J. Hum. Genet.,2000
5. Mutations in GJB6 cause nonsyndromic autosomal dominant deafness at DFNA3 locus;Grifa;Nat. Genet.,1999
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