Pediatric Neurology Briefs (Nov 2002)

Mitochondrial DNA Depletion Syndrome

  • J Gordon Millichap

DOI
https://doi.org/10.15844/pedneurbriefs-16-11-3
Journal volume & issue
Vol. 16, no. 11
pp. 82 – 83

Abstract

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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.

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