Response to "Leigh-like syndrome with mild mtDNA depletion due to the SUCLG1 variant c.626C>A"
Publication year
2018Source
Molecular Genetics and Metabolism Reports, 13, 18, (2018), pp. 10ISSN
Publication type
Article / Letter to editor

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Organization
Paediatrics
Laboratory Medicine
Journal title
Molecular Genetics and Metabolism Reports
Volume
vol. 13
Issue
iss. 18
Page start
p. 10
Subject
Radboudumc 3: Disorders of movement DCMN: Donders Center for Medical NeuroscienceThis item appears in the following Collection(s)
- Academic publications [229134]
- Electronic publications [111496]
- Faculty of Medical Sciences [87758]
- Open Access publications [80319]
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