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No clinical trials have been registered for mitochondrial complex 5 (ATP synthase) deficiency, mitochondrial type 1.
5 publications have been identified in PubMed for mitochondrial complex 5 (ATP synthase) deficiency, mitochondrial type 1. Research spans Case Report / Case Series (40%), Basic Science / Preclinical (40%), and Review / Meta-Analysis (20%).
Feofilaktova T (2025). [PMID: 40761376](https://pubmed.ncbi.nlm.nih.gov/40761376/). *Front Mol Neurosci*. [Review / Meta-Analysis]
İpek R (2025). [PMID: 40014158](https://pubmed.ncbi.nlm.nih.gov/40014158/). *Neurogenetics*. [Case Report / Case Series]
Dong H (2025). [PMID: 39878121](https://pubmed.ncbi.nlm.nih.gov/39878121/). *Autophagy*. [Basic Science / Preclinical]
Xian C (2025). [PMID: 41053757](https://pubmed.ncbi.nlm.nih.gov/41053757/). *J Transl Med*. [Case Report / Case Series]
Wojcicki K (2024). [PMID: 39126062](https://pubmed.ncbi.nlm.nih.gov/39126062/). *Int J Mol Sci*. [Basic Science / Preclinical]
Data assembled from 3 of 12 sources · Last updated Sep 19, 2026, 11:56 AM UTC
Online Mendelian Inheritance in Man