Favourable clinical course in an infant with severe deficiency of complex III of the respiratory chain combined with less severe deficiency of complexes I, II and IV
Publication year
1997Source
European Journal of Pediatrics, 156, (1997), pp. 931-934ISSN
Publication type
Article / Letter to editor

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Organization
Paediatrics - OUD tm 2017
Neurology
Human Genetics
Journal title
European Journal of Pediatrics
Volume
vol. 156
Page start
p. 931
Page end
p. 934
Subject
Clinical aspects of mitochondriocytopathies; Neuromuscular and neurometabolic disorders; Analysis of mitochondrial DNA as part of the diagnosis of mitochondrial myopathies; Klinische aspecten van mitochondriocytopathieën; Neuromusculaire en neurometabole aandoeningen; Onderzoek van mitochondrieel DNA in het kader van diagnostiek van mitochondriële myopathieenThis item appears in the following Collection(s)
- Academic publications [227727]
- Faculty of Medical Sciences [86204]
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