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Mitochondrial complex II deficiency due to pathogenic variants in the SDHC gene, resulting in a variety of clinical manifestations, including neurological and muscular symptoms.
No clinical trials have been registered for SDHC-related Mitochondrial Disease.
2 publications have been identified in PubMed for SDHC-related Mitochondrial Disease. Research spans Basic Science / Preclinical (100%).
Sanadgol N (2025). [PMID: 40581642](https://pubmed.ncbi.nlm.nih.gov/40581642/). *Cell Biosci*. [Basic Science / Preclinical]
Dai Y (2024). [PMID: 38877845](https://pubmed.ncbi.nlm.nih.gov/38877845/). *FASEB J*. [Basic Science / Preclinical]
Data assembled from 2 of 12 sources · Last updated Sep 19, 2026, 4:32 PM UTC
Common questions about SDHC-related Mitochondrial Disease