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Any mitochondrial complex I deficiency in which the cause of the disease is a mitochondrial mutation in the complex I subunit genes.
No clinical trials have been registered for mitochondrial complex I deficiency, mitochondrial type.
14 publications have been identified in PubMed for mitochondrial complex I deficiency, mitochondrial type. Research spans Case Report / Case Series (50%), Basic Science / Preclinical (36%), and Other (7%).
Research Type | Count | % of Total |
|---|---|---|
Patient case studies | 7 | 50% |
Laboratory research | 5 | 36% |
Other research | 1 | 7% |
Research summaries | 1 | 7% |
Deng Y (2026). [PMID: 41967292](https://pubmed.ncbi.nlm.nih.gov/41967292/). *Redox Biol*. [Basic Science / Preclinical]
Data assembled from 2 of 12 sources · Last updated Sep 20, 2026, 9:39 AM UTC
Mantecon M (2026). [PMID: 41981912](https://pubmed.ncbi.nlm.nih.gov/41981912/). *HGG Adv*. [Basic Science / Preclinical]
Yang Q (2026). [PMID: 41982415](https://pubmed.ncbi.nlm.nih.gov/41982415/). *Front Neurol*. [Case Report / Case Series]
Yuan JH (2026). [PMID: 41361485](https://pubmed.ncbi.nlm.nih.gov/41361485/). *J Hum Genet*. [Case Report / Case Series]
Kalantari S (2025). [PMID: 39821332](https://pubmed.ncbi.nlm.nih.gov/39821332/). *Am J Med Genet A*. [Case Report / Case Series]
Giguet-Valard AG (2025). [PMID: 40806260](https://pubmed.ncbi.nlm.nih.gov/40806260/). *Int J Mol Sci*. [Case Report / Case Series]
Kaiyrzhanov R (2025). [PMID: 39963288](https://pubmed.ncbi.nlm.nih.gov/39963288/). *Brain Commun*. [Other]
Haddad S (2025). [PMID: 40207266](https://pubmed.ncbi.nlm.nih.gov/40207266/). *Oxf Med Case Reports*. [Case Report / Case Series]
Chen H (2025). [PMID: 40990041](https://pubmed.ncbi.nlm.nih.gov/40990041/). *Adv Sci (Weinh)*. [Basic Science / Preclinical]
Shi Y (2025). [PMID: 39612123](https://pubmed.ncbi.nlm.nih.gov/39612123/). *Clin Transl Oncol*. [Basic Science / Preclinical]