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Epigenetics in Prader-Willi Syndrome

Prader-Willi Syndrome (PWS) is a rare neurodevelopmental disorder that affects approximately 1 in 20,000 individuals worldwide. Symptom progression in PWS is classically characterized by two nutritional stages. Stage 1 is hypotonia characterized by poor muscle tone that leads to poor feeding behavio...

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Detalles Bibliográficos
Autores principales:	Mendiola, Aron Judd P., LaSalle, Janine M.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Frontiers Media S.A. 2021
Materias:	Genetics
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7917289/ https://www.ncbi.nlm.nih.gov/pubmed/33659026 http://dx.doi.org/10.3389/fgene.2021.624581

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