Mitochondrial DNA Depletion Syndrome

J Gordon Millichap

doi:10.15844/pedneurbriefs-16-11-3

Mitochondrial DNA Depletion Syndrome

Pediatric Neurology Briefs

Volume 16 (2002): Issue 11

By: J Gordon Millichap

Open Access

|Nov 2002

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.

References

Mancuso M Salviati L Sacconi S Otaegui D Camaño P Marina A Mitochondrial DNA depletion: mutations in thymidine kinase gene with myopathy and SMA Neurology 2002 Oct 59 8 1197 1202 10.1212/01.WNL.0000028689.93049.9A 12391347
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Articles in this issue

DOI: https://doi.org/10.15844/pedneurbriefs-16-11-3 | Journal eISSN: 2166-6482

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Language: English

Page range: 82 - 83

Published on: Nov 1, 2002

Published by: Pediatric Neurology Briefs Publishers

In partnership with: Paradigm Publishing Services

Keywords:

Myopathic Mitochondrial DNA Depletion Syndrome,

Thymidine Kinase 2,

Deoxyribonucleotide Metasbolism

© 2002 J Gordon Millichap, published by Pediatric Neurology Briefs Publishers
This work is licensed under the Creative Commons Attribution 4.0 License.

Volume 16 (2002): Issue 11