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dc.contributor.authorJ. Gordon Millichap
dc.contributor.otherDivision of Neurology, Ann & Robert H. Lurie Children’s Hospital of Chicago, Chicago, IL; and Departments of Pediatrics and Neurology, Northwestern University Feinberg School of Medicine, Chicago, IL
dc.date.accessioned2015-10-16T04:00:37Z
dc.date.available2025-10-02T03:27:55Z
dc.date.issued01-10-2015
dc.identifier.issn-
dc.identifier.urihttps://www.pediatricneurologybriefs.com/articles/217
dc.description.abstractInvestigators at the National Hospital for Neurology and Neurosurgery, Queen Square, London, and multiple centers in the UK, Europe, US, Melbourne, Australia, and Canada, analyzed ECG recordings of 52 patients with alternating hemiplegia from 9 countries; all had whole-exome, whole-genome, or direct Sanger sequencing of ATP1A3; 47 had a confirmed missense mutation in ATP1A3.
dc.format-
dc.language.isoEN
dc.publisherPediatric Neurology Briefs Publishers
dc.relation.uri['https://journals.asm.org/writing-your-paper?journal=jb', 'https://journals.asm.org/waivers', 'https://journals.asm.org/journal/jb/scope', 'https://journals.asm.org/journal/jb']
dc.rightsCC BY
dc.subject['molecular mechanisms', 'bacterial physiology', 'archaea', 'bacteriophages', 'host-microbe interactions', 'environmental microbiology', 'Medicine', 'R']
dc.subject.lccPediatrics
dc.titleAlternating Hemiplegia and Cardiac Dysrhythmia
dc.typeArticle
dc.description.keywordsalternating hemiplegia of childhood
dc.description.keywordsatp1a3
dc.description.keywordssudep
dc.description.pages-
dc.description.doi10.15844/pedneurbriefs-29-9-6
dc.title.journalPediatric Neurology Briefs
dc.identifier.e-issn2166-6482
dc.identifier.oaioai:doaj.org/journal:949aeddc8b524e178f478245d282fd8a
dc.journal.infoVolume 29, Issue 9


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