Mutations in ATP1A3 cause alternating hemiplegia of childhood

Please use this identifier to cite or link to this item: https://doi.org/10.1111/cge.12031

DC Field	Value
dc.title	Mutations in ATP1A3 cause alternating hemiplegia of childhood
dc.contributor.author	Aminkeng, F
dc.date.accessioned	2022-12-05T03:28:28Z
dc.date.available	2022-12-05T03:28:28Z
dc.date.issued	2013-01-01
dc.identifier.citation	Aminkeng, F (2013-01-01). Mutations in ATP1A3 cause alternating hemiplegia of childhood. CLINICAL GENETICS 83 (1) : 32-33. ScholarBank@NUS Repository. https://doi.org/10.1111/cge.12031
dc.identifier.issn	0009-9163
dc.identifier.issn	1399-0004
dc.identifier.uri	https://scholarbank.nus.edu.sg/handle/10635/235311
dc.description.abstract	Heterozygous de novo mutations in ATP1A3 in patients with alternating hemiplegia of childhood: a whole-exome sequencing gene-identification study. Rosewich et al. (2012) Lancet Neurology 11(9):764-773. © 2012 John Wiley & Sons A/S. Published by Blackwell Publishing Ltd.
dc.language.iso	en
dc.publisher	WILEY
dc.source	Elements
dc.subject	Science & Technology
dc.subject	Life Sciences & Biomedicine
dc.subject	Genetics & Heredity
dc.subject	ONSET
dc.type	Editorial
dc.date.updated	2022-11-30T19:43:59Z
dc.contributor.department	MEDICINE
dc.description.doi	10.1111/cge.12031
dc.description.sourcetitle	CLINICAL GENETICS
dc.description.volume	83
dc.description.issue	1
dc.description.page	32-33
dc.published.state	Published
Appears in Collections:	Staff Publications Elements

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