Due to necessary maintenance, Xenbase will be unavailable December 24-30, 2014. We apologize for the inconvenience.

Click on this message to dismiss it.
Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
XB-ART-12405
Nat Genet. September 1, 1999; 23 (1): 16-8.

Mutations in GJB6 cause nonsyndromic autosomal dominant deafness at DFNA3 locus.

Grifa A , Wagner CA , D'Ambrosio L , Melchionda S , Bernardi F , Lopez-Bigas N , Rabionet R , Arbones M , Monica MD , Estivill X , Zelante L , Lang F , Gasparini P .



PubMed ID: 10471490
Article link: Nat Genet.

Genes referenced: gjb2
Antibodies referenced:
Morpholinos referenced:

My Xenbase: [ Log-in / Register ]
version: [3.3.1]


Major funding for Xenbase is provided by the National Institute of Child Health and Human Development, grant P41 HD064556