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A cytochrome-c oxidase deficiency disease characterized by localization to tissues of the skeletal muscles.
No clinical trials have been registered for COX deficiency, benign infantile mitochondrial myopathy.
3 publications have been identified in PubMed for COX deficiency, benign infantile mitochondrial myopathy. Research spans Case Report / Case Series (67%) and Review / Meta-Analysis (33%).
Buhl E (2025). [PMID: 40210596](https://pubmed.ncbi.nlm.nih.gov/40210596/). *Clinical genetics*. [Case Report / Case Series]
Adorisio R (2025). [PMID: 40678571](https://pubmed.ncbi.nlm.nih.gov/40678571/). *Frontiers in cardiovascular medicine*. [Review / Meta-Analysis]
Ma YT (2025). [PMID: 40008317](https://pubmed.ncbi.nlm.nih.gov/40008317/). *Case reports in medicine*. [Case Report / Case Series]
Data assembled from 2 of 12 sources · Last updated Sep 19, 2026, 9:42 PM UTC
Common questions about COX deficiency, benign infantile mitochondrial myopathy