Leigh syndrome associated with a mutation in the NDUFS7 (PSST) nuclear encoded subunit of complex I.
Publication year
1999Author(s)
Number of pages
4 p.
Source
Annals of Neurology, 45, (1999), pp. 787-790ISSN
Publication type
Article / Letter to editor
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Organization
Paediatrics - OUD tm 2017
Tumorimmunology
Human Genetics
Journal title
Annals of Neurology
Volume
vol. 45
Page start
p. 787
Page end
p. 790
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 [244128]
- Faculty of Medical Sciences [92874]
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