Cerebral palsy and pyruvate dehydrogenase deficiency: identification of two new mutations in the E1alpha gene.
Publication year
2000Author(s)
Number of pages
5 p.
Source
European Journal of Pediatrics, 158, (2000), pp. 853-857ISSN
Publication type
Article / Letter to editor

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Organization
Paediatrics - OUD tm 2017
Journal title
European Journal of Pediatrics
Volume
vol. 158
Page start
p. 853
Page end
p. 857
Subject
Molecular genetic studies of mitochondriocytopathies; Moleculair genetisch onderzoek van mitochondriopathieënThis item appears in the following Collection(s)
- Academic publications [227207]
- Faculty of Medical Sciences [86711]
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