Retinal cadherins and the retinal cadherinopathies: Current concepts and future directions
Author:
Funder
National Institute for Health and Care Research
Medical Research Council
Publisher
Elsevier BV
Subject
Sensory Systems,Ophthalmology
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3. PCDH15 is expressed in the neurosensory epithelium of the eye and ear and mutant alleles are responsible for both USH1F and DFNB23;Ahmed;Hum. Mol. Genet.,2003
4. Gene structure and mutant alleles of PCDH15: nonsyndromic deafness DFNB23 and type 1 Usher syndrome;Ahmed;Hum. Genet.,2008
5. The mouse Ames waltzer hearing-loss mutant is caused by mutation of Pcdh15, a novel protocadherin gene;Alagramam;Nat. Genet.,2001
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