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Longitudinal course of epilepsy in Rett syndrome and related disorders

Epilepsy is common in Rett syndrome, an X-linked dominant disorder caused by mutations in the MECP2 gene, and in Rett-related disorders, such as MECP2 duplication. However, neither the longitudinal course of epilepsy nor the patterns of seizure onset and remission have been described in Rett syndrom...

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Salvato in:
Dettagli Bibliografici
Pubblicato in:Brain
Autori principali: Tarquinio, Daniel C, Hou, Wei, Berg, Anne, Kaufmann, Walter E, Lane, Jane B, Skinner, Steven A, Motil, Kathleen J, Neul, Jeffrey L, Percy, Alan K, Glaze, Daniel G
Natura: Artigo
Lingua:Inglês
Pubblicazione: Oxford University Press 2017
Soggetti:
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC5278305/
https://ncbi.nlm.nih.gov/pubmed/28007990
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/brain/aww302
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