| Gene Symbol | NDUFA13 |
| Protein Type | Gene |
| Function | ### Structural Role in Complex I |
| GeneCards | NDUFA13 |
| Human Protein Atlas | NDUFA13 |
| Leigh Syndrome | A severe neurodegenerative disorder presenting with developmental regression, hypotonia, ataxia, and characteristic lesions in the brainstem and basal ganglia [@leigh_syndrome] |
| Cardiomyopathy | Hypertrophic or dilated cardiomyopathy due to cardiac muscle energy failure |
| Encephalomyopathy | Combined neurological and muscular involvement |
| Growth Retardation | Failure to thrive due to impaired energy metabolism |
| Associated Diseases | neurodegeneration |
| Databases | GeneCardsUniProtNCBI GeneHPASTRING |
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