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Any mitochondrial complex I deficiency, mitochondrial type, in which the cause of the disease is a mutation in the MTND3 gene.
No clinical trials have been registered for mitochondrial complex I deficiency, mitochondrial type 1.
8 publications have been identified in PubMed for mitochondrial complex I deficiency, mitochondrial type 1. Research spans Case Report / Case Series (38%), Basic Science / Preclinical (38%), and Other (13%).
Vetha BSS (2026). [PMID: 42147162](https://pubmed.ncbi.nlm.nih.gov/42147162/). *Res Sq*. [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]
Burg L (2025). [PMID: 40786033](https://pubmed.ncbi.nlm.nih.gov/40786033/). *Front Pharmacol*. [Basic Science / Preclinical]
Kaiyrzhanov R (2025). [PMID: 39963288](https://pubmed.ncbi.nlm.nih.gov/39963288/). *Brain Commun*. [Other]
Data assembled from 3 of 12 sources · Last updated Sep 21, 2026, 11:06 AM UTC
Online Mendelian Inheritance in Man
Haddad S (2025). [PMID: 40207266](https://pubmed.ncbi.nlm.nih.gov/40207266/). *Oxf Med Case Reports*. [Case Report / Case Series]
Flønes IH (2024). [PMID: 38684731](https://pubmed.ncbi.nlm.nih.gov/38684731/). *Nat Commun*. [Basic Science / Preclinical]