The N-terminal domain of the Schaaf–Yang syndrome protein MAGEL2 likely has a role in RNA metabolism

MAGEL2 encodes the L2 member of the melanoma-associated antigen gene (MAGE) protein family, truncating mutations of which can cause Schaaf-Yang syndrome, an autism spectrum disorder. MAGEL2 is also inactivated in Prader–Willi syndrome, which overlaps clinically and mechanistically with Schaaf–Yang s...

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Detalles Bibliográficos
Autores principales: Sanderson, Matthea R., Fahlman, Richard P., Wevrick, Rachel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Biochemistry and Molecular Biology 2021
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8350409/
https://www.ncbi.nlm.nih.gov/pubmed/34265304
http://dx.doi.org/10.1016/j.jbc.2021.100959

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8350409/
https://www.ncbi.nlm.nih.gov/pubmed/34265304
http://dx.doi.org/10.1016/j.jbc.2021.100959

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