Autosomal Dominant 12 Deafness

mutation in TECTA gene

Also Known As:

Deafness, Autosomal Dominant 12; DFNA12; DFNA8; Deafness, Autosomal Dominant 8

Networked: 1 relevant articles (0 outcomes, 0 trials/studies)

Drugs and Important Biological Agents (IBA) related to Autosomal Dominant 12 Deafness:

1.	NucleotidesIBA 09/01/1999 - "We have studied a Swedish pedigree with autosomal dominant NSHI with possible digenic inheritance of the disease, involving locus DFNA12 in chromosome 11 and locus DFNA2 in chromosome 1. Mutation analysis of the TECTA gene in this family has identified eight nucleotide substitutions indicating that TECTA is highly polymorphic. "