https://pubmed.ncbi.nlm.nih.gov/18319072/
CABC1 gene mutations cause ubiquinone deficiency with cerebellar ataxia and seizures
Coenzyme Q(10) (CoQ(10)) plays a pivotal role in oxidative phosphorylation (OXPHOS) in that it distributes electrons between the various dehydrogenases and the...
cerebellar ataxiagenemutationscauseubiquinone