Cardiac autonomic control in Rett syndrome: Insights from heart rate variability analysis

Rett syndrome (RTT) is a rare and severe neurological disorder mainly affecting females, usually linked to methyl-CpG-binding protein 2 (MECP2) gene mutations. Manifestations of RTT typically include loss of purposeful hand skills, gait and motor abnormalities, loss of spoken language, stereotypic h...

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Detalles Bibliográficos
Autores principales: Cordani, Ramona, Tobaldini, Eleonora, Rodrigues, Gabriel Dias, Giambersio, Donatella, Veneruso, Marco, Chiarella, Lorenzo, Disma, Nicola, De Grandis, Elisa, Toschi-Dias, Edgar, Furlan, Ludovico, Carandina, Angelica, Prato, Giulia, Nobili, Lino, Montano, Nicola
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Neuroscience
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10067665/
https://www.ncbi.nlm.nih.gov/pubmed/37021139
http://dx.doi.org/10.3389/fnins.2023.1048278

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10067665/
https://www.ncbi.nlm.nih.gov/pubmed/37021139
http://dx.doi.org/10.3389/fnins.2023.1048278

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