Query author contributions in Reactome

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Details on Person Nijtmans, Leo G

Class:Id	Person:5690010
_displayName	Nijtmans, Leo G
_timestamp	2015-04-27 12:26:40
created	[InstanceEdit:5690025] Jassal, Bijay, 2015-04-27
firstname	Leo G
initial	LG
surname	Nijtmans
(author)	[LiteratureReference:5690017] NUBPL mutations in patients with complex I deficiency and a distinct MRI pattern [LiteratureReference:9865562] A mutation in the FAM36A gene, the human ortholog of COX20, impairs cytochrome c oxidase assembly and is associated with ataxia and muscle hypotonia [LiteratureReference:9865895] Mutations in the UQCC1-interacting protein, UQCC2, cause human complex III deficiency associated with perturbed cytochrome b protein expression [LiteratureReference:9906886] A mutation in the human CBP4 ortholog UQCC3 impairs complex III assembly, activity and cytochrome b stability
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No pathways have been reviewed or authored by Nijtmans, Leo G (5690010)