A nonsynonymous mutation in the WFS1 gene in a Finnish family with age-related hearing impairment
Author:
Funder
Sigrid Juselius Foundation
Medical Research Center
University of Oulu
Oulu University Hospital
Publisher
Elsevier BV
Subject
Sensory Systems
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4. Mutations in the wolfram syndrome 1 gene (WFS1) are a common cause of low frequency sensorineural hearing loss;Bespalova;Hum. Mol. Genet.,2001
5. Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel cadherin-like gene CDH23;Bork;Am. J. Hum. Genet.,2001
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3. Mutation analysis of the WFS1 gene in a Chinese family with autosomal-dominant non-syndrome deafness;Scientific Reports;2022-12-23
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