Sensorineural hearing loss due to a novel mutation in the PCDH15 gene: A case study
Author:
Publisher
Elsevier BV
Subject
General Earth and Planetary Sciences,General Environmental Science
Reference38 articles.
1. The tip-link antigen, a protein associated with the transduction complex of sensory hair cells, is protocadherin-15;Ahmed;J. Neurosci.,2006
2. 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
3. Gene structure and mutant alleles of PCDH15: nonsyndromic deafness DFNB23 and type 1 Usher syndrome;Ahmed;Hum. Genet.,2008
4. Mutations of the protocadherin gene PCDH15 cause usher syndrome type 1F;Ahmed;Am. J. Hum. Genet.,2001
5. Mutations in the novel protocadherin PCDH15 cause Usher syndrome type 1F;Alagramam;Hum. Mol. Genet.,2001
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