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The feasibility of using actigraphy to characterize sleep in Rett syndrome

BACKGROUND: Rett syndrome (RTT) is a neurodevelopmental disorder primarily caused by mutations in the MECP2 gene. Sleep problems are reported by the majority of caregivers of individuals with RTT. METHODS: The present study aimed to replicate and extend previous work about the feasibility of measuri...

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Detalles Bibliográficos
Autores principales:	Merbler, Alyssa M., Byiers, Breanne J., Garcia, John J., Feyma, Timothy J., Symons, Frank J.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BioMed Central 2018
Materias:	Research
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5828406/ https://www.ncbi.nlm.nih.gov/pubmed/29482495 http://dx.doi.org/10.1186/s11689-018-9227-z

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