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leigh syndrome due to mitochondrial complex i deficiency
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FOXRED1
Systematic subcellular localization of novel proteins identified by large-scale cDNA sequencing
NDUFA2
Identification of mitochondrial complex I assembly intermediates by tracing tagged NDUFS3 demonstrates the entry point of mitochondrial subunits
NDUFA9
Human complex I defects can be resolved by monoclonal antibody analysis into distinct subunit assembly patterns
NDUFS3
Respiratory chain complex I deficiency
Human complex I deficiency: clinical spectrum and involvement of oxygen free radicals in the pathogenicity of the defect
A conditional knockout resource for the genome-wide study of mouse gene function
NDUFS8
Genomic structure of the human NDUFS8 gene coding for the iron-sulfur TYKY subunit of the mitochondrial NADH:ubiquinone oxidoreductase