| Literature DB >> 11450843 |
J Akita1, S Abe, H Shinkawa, W J Kimberling, S Usami.
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.Entities:
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Year: 2001 PMID: 11450843 DOI: 10.1007/s100380170053
Source DB: PubMed Journal: J Hum Genet ISSN: 1434-5161 Impact factor: 3.172