A MAGEL2-deubiquitinase complex modulates the ubiquitination of circadian rhythm protein CRY1.
MAGEL2 encodes the L2 member of the MAGE (melanoma antigen) protein family. Protein truncating mutations in MAGEL2 cause Schaaf-Yang syndrome, and MAGEL2 is one of a small set of genes deleted in Prader-Willi syndrome. Excessive daytime sleepiness, night-time or early morning waking, and narcoleptic...
Main Authors: | K Vanessa Carias, Mercedes Zoeteman, Abigail Seewald, Matthea R Sanderson, Jocelyn M Bischof, Rachel Wevrick |
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Format: | Article |
Language: | English |
Published: |
Public Library of Science (PLoS)
2020-01-01
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Series: | PLoS ONE |
Online Access: | https://doi.org/10.1371/journal.pone.0230874 |
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