Reply: NAD(P)HX dehydratase protein-truncating mutations are associated with neurodevelopmental disorder exacerbated by acute illness

Reference : Reply: NAD(P)HX dehydratase protein-truncating mutations are associated with neurodev...


	Document type :	Scientific journals : Article
	Discipline(s) :	Life sciences : Biochemistry, biophysics & molecular biology
	Focus Areas :	Systems Biomedicine
	To cite this reference:	http://hdl.handle.net/10993/44395

Title :	Reply: NAD(P)HX dehydratase protein-truncating mutations are associated with neurodevelopmental disorder exacerbated by acute illness
Language :	English
Author, co-author :	Van Bergen, Nicole J. [The Royal Children's Hospital > Murdoch Children's Research Institute]
	Linster, Carole [University of Luxembourg > Luxembourg Centre for Systems Biomedicine (LCSB) > >]
	Christodoulou, John [The Royal Children's Hospital > Murdoch Children's Research Institute]
Publication date :	27-May-2020
Journal title :	Brain: a Journal of Neurology
Publisher :	Oxford University Press
Volume :	143
Issue/season :	7
Pages :	e55
Peer reviewed :	Yes (verified by ORBi^lu)
Audience :	International
ISSN :	0006-8950
e-ISSN :	1460-2156
City :	Oxford
Country :	United Kingdom
Permalink :	http://hdl.handle.net/10993/44395
DOI :	10.1093/brain/awaa131

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Limited access	Van Bergen et al 2020.pdf		Publisher postprint	200.65 kB	Request a copy

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