Mitochondrial Complex I Deficiency, Nuclear Type 13 (MC1DN13)

Alias:

Mc1dn13

Mitochondrial Complex 1 Deficiency, Nuclear Type 13

Nuclear Type Mitochondrial Complex I Deficiency 13

Mi Complex I Deficiency, Nuclear Type 13

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Mitochondrial Complex I Deficiency, Nuclear Type 13, is also known as mc1dn13. An important gene associated with Mitochondrial Complex I Deficiency, Nuclear Type 13 is NDUFA2 (NADH:Ubiquinone Oxidoreductase Subunit A2). Affiliated tissues include liver and brain, and related phenotypes are intellectual disability and developmental regression

Related ID：

MALACARDS：MTC160

OMIM：618235

MESH：D028361