Patients with PWS and related syndromes display differentially methylated regions involved in neurodevelopmental and nutritional trajectory

BACKGROUND: Prader–Willi syndrome is a rare genetic neurodevelopmental disorder caused by a paternal deficiency of maternally imprinted gene expression located in the chromosome 15q11–q13 region. Previous studies have demonstrated that several classes of neurodevelopmental disorders can be attribute...

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Detalles Bibliográficos
Autores principales: Salles, Juliette, Eddiry, Sanaa, Lacassagne, Emmanuelle, Laurier, Virginie, Molinas, Catherine, Bieth, Éric, Franchitto, Nicolas, Salles, Jean-Pierre, Tauber, Maithé
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8361855/
https://www.ncbi.nlm.nih.gov/pubmed/34389046
http://dx.doi.org/10.1186/s13148-021-01143-0

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8361855/
https://www.ncbi.nlm.nih.gov/pubmed/34389046
http://dx.doi.org/10.1186/s13148-021-01143-0

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