Genes and syndromic hearing loss
Author:
Publisher
Elsevier BV
Subject
LPN and LVN,Speech and Hearing,Cognitive Neuroscience,Linguistics and Language,Experimental and Cognitive Psychology
Reference29 articles.
1. Mutations of the protocadherin gene PCDH15 cause Usher syndrome type 1F;Ahmed;American Journal of Human Genetics,2001
2. The mouse Ames waltzer hearing loss mutant is caused by mutation of Pcdh15, a novel protocadherin gene;Alagramam;Nature Genetics,2001
3. An exonic mutation in the HuP2 paired domain gene causes Waardenburg’s syndrome;Baldwin;Nature,1992
4. Identification of mutations in the COL4A5 collagen gene in Alport syndrome;Barker;Science,1990
5. A recessive contiguous gene deletion syndrome causing infantile hyperinsulinism, enteropathy and deafness identifies the Usher type 1C gene;Bitner-Glindzicz;Nature Genetics,2000
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