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....
Guardado en:
| Autores principales: | , , , , , |
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| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
Elsevier
2025-04-01
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| Colección: | HGG Advances |
| Materias: | |
| Acceso en línea: | http://www.sciencedirect.com/science/article/pii/S2666247725000260 |
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