Comorbidity of GJB2 and WFS1 mutations in one family
Author:
Publisher
Elsevier BV
Subject
Genetics,General Medicine
Reference27 articles.
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2. Mutations in the Wolfram syndrome 1 gene (WFS1) are a common cause of low frequency sensorineural hearing loss;Bespalova;Hum. Mol. Genet.,2001
3. Autosomal dominant low-frequency hearing impairment (DFNA6/14): a clinical and genetic family study;Bom;Otol. Neurotol.,2002
4. Further evidence for linkage of low–mid frequency hearing impairment to the candidate region on chromosome 4p16.3;Brodwolf;Clin. Genet.,2001
5. Mutational spectrum of the WFS1 gene in Wolfram syndrome, nonsyndromic hearing impairment, diabetes mellitus, and psychiatric disease;Cryns;Hum. Mutat.,2003
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1. Hearing impairment caused by mutations in two different genes responsible for nonsyndromic and syndromic hearing loss within a single family;Journal of Applied Genetics;2017-11-18
2. The Application of Next-Generation Sequencing for Mutation Detection in Autosomal-Dominant Hereditary Hearing Impairment;Otology & Neurotology;2017-07
3. WFS1andGJB2mutations in patients with bilateral low-frequency sensorineural hearing loss;The Laryngoscope;2017-03-08
4. New Trends in Research and Clinical Practice for Congenital Hearing Loss Caused by Gene Mutations;The Japan Journal of Logopedics and Phoniatrics;2015
5. Targeted genomic capture and massively parallel sequencing to identify novel variants causing Chinese hereditary hearing loss;Journal of Translational Medicine;2014-11-12
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