Mutated SUCLG1 causes mislocalization of SUCLG2 protein, morphological alterations of mitochondria and an early-onset severe neurometabolic disorder

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Publication year
2019Source
Molecular Genetics and Metabolism, 126, 1, (2019), pp. 43-52ISSN
Publication type
Article / Letter to editor

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Organization
Paediatrics
Laboratory Medicine
Journal title
Molecular Genetics and Metabolism
Volume
vol. 126
Issue
iss. 1
Page start
p. 43
Page end
p. 52
Subject
All institutes and research themes of the Radboud University Medical Center; Radboudumc 11: Renal disorders RIMLS: Radboud Institute for Molecular Life Sciences; Radboudumc 3: Disorders of movement DCMN: Donders Center for Medical Neuroscience; Radboudumc 6: Metabolic Disorders RIMLS: Radboud Institute for Molecular Life SciencesThis item appears in the following Collection(s)
- Academic publications [204994]
- Electronic publications [103280]
- Faculty of Medical Sciences [81051]
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