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ENMitochondrial Complex I Deficiency, Nuclear Type 17 (MC1DN17)
Alias:
Mc1dn17
Mitochondrial Complex 1 Deficiency, Nuclear Type 17
Nuclear Type Mitochondrial Complex I Deficiency 17
Mi Complex I Deficiency, Nuclear Type 17
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Mitochondrial Complex I Deficiency, Nuclear Type 17, is also known as mc1dn17. An important gene associated with Mitochondrial Complex I Deficiency, Nuclear Type 17 is NDUFAF6 (NADH:Ubiquinone Oxidoreductase Complex Assembly Factor 6). Affiliated tissues include liver and skeletal muscle, and related phenotypes are scoliosis and dysarthria
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