The xchroomosomal NDUFA1 gene of complex I in mitochondrial encephalomyopathies: tissue expression and mutation detection
Publication year
1998Author(s)
Number of pages
6 p.
Source
Journal of Inherited Metabolic Disease, 21, (1998), pp. 210-215ISSN
Publication type
Article / Letter to editor

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Organization
Paediatrics - OUD tm 2017
Human Genetics
Journal title
Journal of Inherited Metabolic Disease
Volume
vol. 21
Page start
p. 210
Page end
p. 215
Subject
Molecular genetic studies of mitochondriocytopathies; Analysis of mitochondrial DNA as part of the diagnosis of mitochondrial myopathies; Moleculair genetisch onderzoek van mitochondriopathieën; Onderzoek van mitochondrieel DNA in het kader van diagnostiek van mitochondriële myopathieenThis item appears in the following Collection(s)
- Academic publications [226902]
- Faculty of Medical Sciences [86456]
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