| Literature DB >> 17485248 |
Catarina M Quinzii1, Michio Hirano, Salvatore DiMauro.
Abstract
Deficiency of Coenzyme Q10 (CoQ10) in muscle has been associated with a spectrum of diseases including infantile-onset multi-systemic diseases, encephalomyopathies with recurrent myobinuria, cerebellar ataxia, and pure myopathy. CoQ10 deficiency predominantly affects children, but patients have presented with adult-onset cerebellar ataxia or myopathy. Mutations in the CoQ10 biosynthetic genes, COQ2 and PDSS2, have been identified in children with the infantile form of CoQ10 deficiency; however, the molecular genetic bases of adult-onset CoQ10 deficiency remains undefined.Entities:
Mesh:
Substances:
Year: 2007 PMID: 17485248 PMCID: PMC2001314 DOI: 10.1016/j.mito.2007.03.004
Source DB: PubMed Journal: Mitochondrion ISSN: 1567-7249 Impact factor: 4.160