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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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| Pubblicato in: | Orphanet J Rare Dis |
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| Autori principali: | , , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
BioMed Central
2016
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4855770/ https://ncbi.nlm.nih.gov/pubmed/27146299 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13023-016-0438-7 |
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