Mitochondrial Complex I Deficiency, Nuclear Type 32 (MC1DN32)

Mitochondrial Complex I Deficiency, Nuclear Type 32, is also known as mc1dn32. An important gene associated with Mitochondrial Complex I Deficiency, Nuclear Type 32 is NDUFB8 (NADH:Ubiquinone Oxidoreductase Subunit B8). Affiliated tissues include liver and skeletal muscle, and related phenotypes are global developmental delay and increased serum lactate