Molecular Changes in Prader-Willi Syndrome Neurons Reveals Clues About Increased Autism Susceptibility

Background: Prader-Willi syndrome (PWS) is a neurodevelopmental disorder characterized by hormonal dysregulation, obesity, intellectual disability, and behavioral problems. Most PWS cases are caused by paternal interstitial deletions of 15q11.2-q13.1, while a smaller number of cases are caused by ch...

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Detalles Bibliográficos
Autores principales: Victor, A. Kaitlyn, Donaldson, Martin, Johnson, Daniel, Miller, Winston, Reiter, Lawrence T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Molecular Neuroscience
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8586424/
https://www.ncbi.nlm.nih.gov/pubmed/34776864
http://dx.doi.org/10.3389/fnmol.2021.747855

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8586424/
https://www.ncbi.nlm.nih.gov/pubmed/34776864
http://dx.doi.org/10.3389/fnmol.2021.747855

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