Missense variants in NOX1 and p22phox in a case of very-early-onset inflammatory bowel disease are functionally linked to NOD2

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Title:	Missense variants in NOX1 and p22phox in a case of very-early-onset inflammatory bowel disease are functionally linked to NOD2
Author(s):	Lipinski, Simone; Petersen, Britt-Sabina; Barann, Matthias; Piecyk, Agnes; Tran, Florian; Mayr, Gabriele; Gilissen, C.F. ; Veltman, J.A. ; Franke, Andre; Rosenstiel, Philip
Publication year:	2019
Source:	Cold Spring Harbor Molecular Case Studies, vol. 5, iss. 1, (2019), article a002428
ISSN:	2373-2873
DOI:	https://doi.org/10.1101/mcs.a002428
Publication type:	Article / Letter to editor
Please use this identifier to cite or link to this item : https://hdl.handle.net/2066/201167
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Subject:	All institutes and research themes of the Radboud University Medical Center Radboudumc 6: Mitochondrial diseases RIMLS: Radboud Institute for Molecular Life Sciences Radboudumc 7: Neurodevelopmental disorders DCMN: Donders Center for Medical Neuroscience
Organization:	Human Genetics
Journal title:	Cold Spring Harbor Molecular Case Studies
Volume:	vol. 5
Issue:	iss. 1
Article number:	a002428