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Circadian rhythm defects in Prader-Willi syndrome neurons

Summary: Prader-Willi syndrome (PWS) is a neurodevelopmental disorder characterized by a spectrum of symptoms, including developmental delay, intellectual disability, and increased risk of autism. PWS is an imprinting disorder caused by the loss of paternal expression of critical genes in the 15q11....

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Principais autores: A. Kaitlyn Victor, Tayler Hedgecock, Chidambaram Ramanathan, Yang Shen, Andrew C. Liu, Lawrence T. Reiter
Formato: Artigo
Idioma:Inglês
Publicado em: Elsevier 2025-04-01
coleção:HGG Advances
Assuntos:
Prader-Willi syndrome
excessive daytime sleepiness
circadian rhythm
dental pulp stem cells
hypersomnolence
sleep disorder
Acesso em linha:http://www.sciencedirect.com/science/article/pii/S2666247725000260
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