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Summary Literature (0)
MIM:618252 - MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 32; MC1DN32

Xenbase Genes:

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0032635 - mitochondrial complex I deficiency, nuclear type 32

Disease Ontology (DO):
DOID:0112080 - nuclear type mitochondrial complex I deficiency 32