A novel splice site mutation in DFNA5 causes late-onset progressive non-syndromic hearing loss in a Chinese family
Author:
Publisher
Elsevier BV
Subject
Otorhinolaryngology,General Medicine,Pediatrics, Perinatology and Child Health
Reference14 articles.
1. The genetics of congenital deafness;Fraser;Otolaryng. Clin. N. Am.,1971
2. Newborn hearing screening–a silent revolution;Morton;New. Engl. J. Med.,2006
3. Genetic epidemiology of hearing impairment;Morton;Ann. NY. Acad. Sci.,1991
4. Nonsyndromic hearing impairment is associated with a mutation in DFNA5;Van Laer;Nat. Genet.,1998
5. A novel mutation identified in the DFNA5 gene in a Dutch family: a clinical and genetic evaluation;Bischoff;Audiol. Neuro-Otol.,2004
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4. Analysis of NFKB1 and NFKB2 gene expression in the blood of patients with sudden sensorineural hearing loss;International Journal of Pediatric Otorhinolaryngology;2023-03
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