Treatment with Oral ATP decreases alternating hemiplegia of childhood with de novo ATP1A3 Mutation

BACKGROUND: Alternating hemiplegia of childhood is an intractable neurological disorder characterized by recurrent episodes of alternating hemiplegia accompanied by other paroxysmal symptoms. Recent research has identified mutations in the ATP1A3 gene as the underlying cause. Adenosine-5'-triph...

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Detalles Bibliográficos
Autores principales: Ju, Jun, Hirose, Shinichi, Shi, Xiu-Yu, Ishii, Atsushi, Hu, Lin-Yan, Zou, Li-Ping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4855770/
https://www.ncbi.nlm.nih.gov/pubmed/27146299
http://dx.doi.org/10.1186/s13023-016-0438-7

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4855770/
https://www.ncbi.nlm.nih.gov/pubmed/27146299
http://dx.doi.org/10.1186/s13023-016-0438-7

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