Mitochondrial complex I deficiency, nuclear type
MONDO:0100223Any mitochondrial complex I deficiency in which the cause of the disease is a mutation in the nuclear-encoded genes that encode structural subunits or assembly factors of complex I.
13 clinical trials for this condition and its sub-types, 0 tagged with Mitochondrial complex I deficiency, nuclear type itself.
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Browse by category →Sub-types of Mitochondrial complex I deficiency, nuclear type
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2 sub-types
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