Back to Search Start Over

Clinical and genetic features of nonsyndromic autosomal dominant sensorineural hearing loss: KCNQ4 is a gene responsible in Japanese.

Authors :
Akita, J.
Abe, S.
Shinkawa, H.
Kimberling, W. J.
Usami, S.
Source :
Journal of Human Genetics. 2001, Vol. 46 Issue 7, p355. 7p.
Publication Year :
2001

Abstract

Sixteen Japanese nonsyndromic autosomal dominant sensorineural hearing loss (ADSNHL) families were investigated clinically as well as genetically. Most families showed postlingual hearing loss. Although the severity of their hearing loss varied, most patients showed mild-moderate sensorineural hearing loss of a progressive nature. Mutation analysis was performed for the MYO7A, KCNQ4, and GJB3 genes, which are known to be responsible for autosomal dominant sensorineural hearing loss. The present study reports that a mutation in KCNQ4, a member of a large family of potassium channel genes, was responsible for ADSNHL in one Japanese family. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
14345161
Volume :
46
Issue :
7
Database :
Academic Search Index
Journal :
Journal of Human Genetics
Publication Type :
Academic Journal
Accession number :
5352413
Full Text :
https://doi.org/10.1007/s100380170053