WDR45 mutations define a novel disease entity - Static Encephalopathy of Childhood with Neurodegeneration in Adulthood

Please use this identifier to cite or link to this item: https://doi.org/10.1111/cge.12183

DC Field	Value
dc.title	WDR45 mutations define a novel disease entity - Static Encephalopathy of Childhood with Neurodegeneration in Adulthood
dc.contributor.author	Aminkeng, F
dc.date.accessioned	2022-12-05T02:54:18Z
dc.date.available	2022-12-05T02:54:18Z
dc.date.issued	2013-09-01
dc.identifier.citation	Aminkeng, F (2013-09-01). WDR45 mutations define a novel disease entity - Static Encephalopathy of Childhood with Neurodegeneration in Adulthood. CLINICAL GENETICS 84 (3) : 209-209. ScholarBank@NUS Repository. https://doi.org/10.1111/cge.12183
dc.identifier.issn	0009-9163
dc.identifier.issn	1399-0004
dc.identifier.uri	https://scholarbank.nus.edu.sg/handle/10635/235308
dc.description.abstract	De novo mutations in the autophagy gene encoding WDR45 cause static encephalopathy of childhood with neurodegeneration in adulthood Saitsu et al. (2013) Nature Genetics 45(4): 445-449 © 2013 John Wiley & Sons A/S.
dc.language.iso	en
dc.publisher	WILEY-BLACKWELL
dc.source	Elements
dc.subject	Science & Technology
dc.subject	Life Sciences & Biomedicine
dc.subject	Genetics & Heredity
dc.type	Editorial
dc.date.updated	2022-11-30T19:05:35Z
dc.contributor.department	MEDICINE
dc.description.doi	10.1111/cge.12183
dc.description.sourcetitle	CLINICAL GENETICS
dc.description.volume	84
dc.description.issue	3
dc.description.page	209-209
dc.published.state	Published
Appears in Collections:	Elements Staff Publications

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