Mitochondrial DNA Depletion Syndrome

Twenty patients with myopathic mitochondrial DNA (mtDNA) depletion syndrome (MDS) were screened for mutations in thymidine kinase 2 (TK2) and deoxyguanosine kinase (dGK) genes at Columbia University, New York, NY.

Dettagli Bibliografici
Autore principale: J Gordon Millichap
Natura: Articolo
Lingua:English
Pubblicazione: Pediatric Neurology Briefs Publishers 2002-11-01
Serie:Pediatric Neurology Briefs
Soggetti:
Accesso online:https://www.pediatricneurologybriefs.com/articles/1561