Pediatric Neurology Briefs
Published 2002 | Version v1.0.0
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Mitochondrial DNA Depletion Syndrome

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Abstract

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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PNB-16-82-b

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Created
2002
When the item was originally created.