A Heterozygous NDUFV1 Variant Aggravates Mitochondrial Complex I Deficiency in a Family with a Homoplasmic ND1 Variant
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Publication year
2018Source
Journal of Pediatrics, 196, (2018), pp. 309-313.e3ISSN
Publication type
Article / Letter to editor
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Organization
Paediatrics
Laboratory Medicine
Internal Medicine
Journal title
Journal of Pediatrics
Volume
vol. 196
Page start
p. 309
Page end
p. 313.e3
Subject
Radboudumc 6: Metabolic Disorders RIMLS: Radboud Institute for Molecular Life Sciences; Internal Medicine - Radboud University Medical Center; Laboratory Medicine - Radboud University Medical Center; Paediatrics - Radboud University Medical Center; Radboud University Medical CenterThis item appears in the following Collection(s)
- Academic publications [245263]
- Electronic publications [132514]
- Faculty of Medical Sciences [93208]
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