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searching for USH1G 4 found (10 total)

alternate case: uSH1G

CDH23 (1,364 words) [view diff] exact match in snippet view article find links to article

Gal A, Ayadi H, Yonekawa H, Petit C (2003). "Usher syndrome type I G (USH1G) is caused by mutations in the gene encoding SANS, a protein that associates

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

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 porphyria

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

USH1C (2,858 words) [view diff] exact match in snippet view article find links to article

Mustapha M, Kikkawa Y, Lainé S, et al. (March 2003). "Usher syndrome type I G (USH1G) is caused by mutations in the gene encoding SANS, a protein that associates