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Mutation in NDUFA13/GRIM19 leads to early onset hypotonia... | ResearchHub
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Mutation in NDUFA13/GRIM19 leads to early onset hypotonia, dyskinesia and sensorial deficiencies, and mitochondrial complex I instability
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Authors
Claire Angebault
16 more
Claire Angebault
•
Bénédicte Camaret
14 more
•
Agathe Roubertie
Published
April 21, 2015
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Journal
Human Molecular Genetics
Topics
Biology
Neuroscience
Medicine
Internal Medicine
Endocrinology
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DOI
10.1093/hmg/ddv133