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Cellular and disease functions of the Prader-Willi Syndrome gene MAGEL2
Melanoma antigen L2 (MAGEL2 or MAGE-L2) is a member of the MAGE family of ubiquitin ligase regulators. It is maternally imprinted and often paternally deleted or mutated in the related neurodevelopmental syndromes, Prader-Willi Syndrome (PWS) and Schaaf-Yang Syndrome (SHFYNG). MAGEL2 is highly expre...
Enregistré dans:
| Publié dans: | Biochem J |
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| Auteurs principaux: | , |
| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
2017
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| Sujets: | |
| Accès en ligne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5594744/ https://ncbi.nlm.nih.gov/pubmed/28626083 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1042/BCJ20160616 |
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