QuickView for SNRPN;jsessionid=738575BADF390F2F631A299E012942A8 (gene)

1. Mosaic de novo SNRPN gene variant associated with Prader-Willi syndrome.
2. The Diagnostic Journey of a Patient with Prader-Willi-Like Syndrome and a Unique Homozygous SNURF-SN…
3. RASSF1A disrupts the NOTCH signaling axis via SNURF/RNF4-mediated ubiquitination of HES1.
4. IGF2R, KCNQ1, PLAGL1, and SNRPN DNA methylation is completed in bovine by the early antral follicle …
5. Accommodative insufficiency in a patient with Prader-Willi syndrome and SNRPN gene mutation.

There were no clinical trials for SNRPN;jsessionid=738575BADF390F2F631A299E012942A8