Usher syndrome: Animal models, retinal function of Usher proteins, and prospects for gene therapy
Author:
Publisher
Elsevier BV
Subject
Sensory Systems,Ophthalmology
Reference106 articles.
1. USH3A transcripts encode clarin-1, a four-transmembrane-domain protein with a possible role in sensory synapses;Adato;European Journal of Human Genetics,2002
2. Mutations of the protocadherin gene PCDH15 cause Usher syndrome type 1F;Ahmed;American Journal of Human Genetics,2001
3. Nonsyndromic recessive deafness DFNB18 and Usher syndrome type IC are allelic mutations of USHIC;Ahmed;Human Genetics,2002
4. The mouse Ames waltzer hearing-loss mutant is caused by mutation of Pcdh15, a novel protocadherin gene;Alagramam;Nature Genetics,2001
5. Mutations in the novel protocadherin PCDH15 cause Usher syndrome type 1F;Alagramam;Human Molecular Genetics,2001
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