Human Gene Discovery for Understanding Development of the Inner Ear and Hearing Loss
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Publisher
Elsevier
Reference99 articles.
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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. The mouse Ames waltzer hearing-loss mutant is caused by mutation of Pcdh15, a novel protocadherin gene;Alagramam;Nat Genet,2001
4. GPSM2 and Chudley-McCullough syndrome: a Dutch founder variant brought to North America;Almomani;Am J Med Genet A,2013
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1. The GPSM2/LGN GoLoco motifs are essential for hearing;Mammalian Genome;2015-12-11
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