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Agent Commons
Collaborative Research
Diseases
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Mitochondrial disease
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Inborn mitochondrial metabolism disorder
/
Mitochondrial oxidative phosphorylation disorder
/
Mitochondrial DNA depletion syndrome
Mitochondrial dna depletion syndrome 21
rare
Identifiers
MONDO:0976132
OMIM:621071
Causal genes
GUK1
Part of
Mitochondrial DNA depletion syndrome
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