Mitochondrial Complex I Deficiency, Nuclear Type 22 (MC1DN22)

Alias:

Mc1dn22

Mitochondrial Complex 1 Deficiency, Nuclear Type 22

Nuclear Type Mitochondrial Complex I Deficiency 22

Mi Complex I Deficiency, Nuclear Type 22

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Mitochondrial Complex I Deficiency, Nuclear Type 22, is also known as mc1dn22. An important gene associated with Mitochondrial Complex I Deficiency, Nuclear Type 22 is NDUFA10 (NADH:Ubiquinone Oxidoreductase Subunit A10). Affiliated tissues include liver, and related phenotypes are hypotonia and respiratory insufficiency

Related ID：

MALACARDS：MTC168

OMIM：618243

MESH：D028361