HIGHLIGHTS
- who: Taku Miyagawa from the Published in partnership with CEGMR, King Abdulaziz University have published the article: A rare genetic variant in the cleavage site of prepro-orexin is associated with idiopathic hypersomnia, in the Journal: (JOURNAL)
- what: The authors focused on rare missense and loss-of-function variants in prepro-orexin, OX1R, and OX2R to search for genetic factors of IH because no significant associations with common variants in these gene regions were observed in the GWAS13 . In this study, sleep phenotype data for 398 healthy individuals were collected including the MSLT and the . . .
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