The human NADH:ubiquinone oxidoreductase NDUFS5 (15kDa) subunit: cDNA cloning, chromosomal localization, tissue distribution and the absence of mutations in isolated complex I-deficient patients.
Publication year
1999Author(s)
Number of pages
10 p.
Source
Journal of Inherited Metabolic Disease, 22, (1999), pp. 19-28ISSN
Publication type
Article / Letter to editor
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Organization
Paediatrics - OUD tm 2017
Journal title
Journal of Inherited Metabolic Disease
Volume
vol. 22
Page start
p. 19
Page end
p. 28
Subject
Molecular genetic studies of mitochondriocytopathies; Moleculair genetisch onderzoek van mitochondriopathieënThis item appears in the following Collection(s)
- Academic publications [243984]
- Faculty of Medical Sciences [92811]
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