Molecular basis of childhood deafness resulting from mutations in the GJB2 (connexin 26) gene.

Rabionet, R

Molecular basis of childhood deafness resulting from mutations in the GJB2 (connexin 26) gene. [electronic resource] - Human genetics Jan 2000 - 40-4 p. digital

Publication Type: Journal Article; Research Support, Non-U.S. Gov't

0340-6717

10.1007/s004390051007 doi


Alleles
Child
Connexin 26
Connexins--genetics
Frameshift Mutation
Gene Deletion
Genes, Recessive
Hearing Loss, Sensorineural--congenital
Humans
Mutation
Mutation, Missense