Histopathology of the Human Inner Ear in a Patient With Sensorineural Hearing Loss Caused by a Variant in DFNA5
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Clinical Neurology,Sensory Systems,Otorhinolaryngology
Reference23 articles.
1. Nonsyndromic hearing impairment is associated with a mutation in DFNA5;Van Laer;Nat Genet,1998
2. A novel mutation identified in the DFNA5 gene in a Dutch family: A clinical and genetic evaluation;Bischoff;Audiol Neurootol,2004
3. A novel DFNA5 mutation, IVS8+4 A>G, in the splice donor site of intron 8 causes late-onset non-syndromic hearing loss in a Chinese family;Cheng;Clin Genet,2007
4. A 3-nucleotide deletion in the polypyrimidine tract of intron 7 of the DFNA5 gene causes nonsyndromic hearing impairment in a Chinese family;Yu;Genomics,2003
5. Evidence for a founder mutation causing DFNA5 hearing loss in East Asians;Park;J Hum Genet,2010
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