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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Bibliographic Details
Main Authors: A. Kaitlyn Victor, Tayler Hedgecock, Chidambaram Ramanathan, Yang Shen, Andrew C. Liu, Lawrence T. Reiter
Format: Article
Language:English
Published: Elsevier 2025-04-01
Series:HGG Advances
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Online Access:http://www.sciencedirect.com/science/article/pii/S2666247725000260
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