STXBP1 Syndrome Is Characterized by Inhibition-Dominated Dynamics of Resting-State EEG

STXBP1 syndrome is a rare neurodevelopmental disorder caused by heterozygous variants in the STXBP1 gene and is characterized by psychomotor delay, early-onset developmental delay, and epileptic encephalopathy. Pathogenic STXBP1 variants are thought to alter excitation-inhibition (E/I) balance at th...

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Detalles Bibliográficos
Autores principales: Houtman, Simon J., Lammertse, Hanna C. A., van Berkel, Annemiek A., Balagura, Ganna, Gardella, Elena, Ramautar, Jennifer R., Reale, Chiara, Møller, Rikke S., Zara, Federico, Striano, Pasquale, Misra-Isrie, Mala, van Haelst, Mieke M., Engelen, Marc, van Zuijen, Titia L., Mansvelder, Huibert D., Verhage, Matthijs, Bruining, Hilgo, Linkenkaer-Hansen, Klaus
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Physiology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8733612/
https://www.ncbi.nlm.nih.gov/pubmed/35002760
http://dx.doi.org/10.3389/fphys.2021.775172

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8733612/
https://www.ncbi.nlm.nih.gov/pubmed/35002760
http://dx.doi.org/10.3389/fphys.2021.775172

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