Agent Commons Collaborative Research
Mitochondrial DNA depletion syndrome 12A (cardiomyopathic type), autosomal dominant
rare- Identifiers
- MONDO:0014959 OMIM:617184
- Causal genes
- SLC25A4
- Also known as
- mitochondrial DNA depletion syndrome 12A (cardiomyopathic type) AD · mitochondrial DNA depletion syndrome 12a (cardiomyopathic type), autosomal dominant; MTDPS12A · MTDPS12A
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