QuickView for USH1G;jsessionid=0FF438AC0C9EE110438662146BECD36F (gene)

1. Novel USH1G homozygous variant underlying USH2-like phenotype of Usher syndrome.
2. SANS (USH1G) regulates pre-mRNA splicing by mediating the intra-nuclear transfer of tri-snRNP comple…
3. Novel digenic inheritance of PCDH15 and USH1G underlies profound non-syndromic hearing impairment.
4. A cryptic sequence targets the adhesion complex scaffold ANKS4B to apical microvilli to promote ente…
5. USH1G with unique retinal findings caused by a novel truncating mutation identified by genome-wide l…

There were no clinical trials for USH1G;jsessionid=0FF438AC0C9EE110438662146BECD36F