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searching for pCDH15 3 found (15 total)

alternate case: PCDH15

USH1G (543 words) [view diff] exact match in snippet view article find links to article

Riazuddin S, Bernstein SL, et al. (2001). "Mutations of the protocadherin gene PCDH15 cause Usher syndrome type 1F". Am. J. Hum. Genet. 69 (1): 25–34. doi:10

List of genetic disorders (995 words) [view diff] exact match in snippet view article find links to article

monosomy 1:2,000-2,500 live female births Usher syndrome MYO7A, USH1C, CDH23, PCDH15, USH1G, USH2A, GPR98, DFNB31, CLRN1 recessive 3-6:100,000 (type I) Variegate

Human genome (10,142 words) [view diff] exact match in snippet view article find links to article

worldwide SMPD1 Usher syndrome 1:23000 in the U.S. 1:28000 in Norway 1:12500 in Germany CDH23, CLRN1, DFNB31, GPR98, MYO7A, PCDH15, USH1C, USH1G, USH2A