POLG mutations associated with Alpers syndrome and mitochondrial DNA depletion
- 29 August 2005
- journal article
- research article
- Published by Wiley in Annals of Neurology
- Vol. 58 (3), 491
- https://doi.org/10.1002/ana.20544
Abstract
No abstract availableThis publication has 3 references indexed in Scilit:
- POLG mutations and Alpers syndromeAnnals of Neurology, 2005
- Infantile hepatocerebral syndromes associated with mutations in the mitochondrial DNA polymerase- ABrain, 2005
- POLG mutations associated with Alpers' syndrome and mitochondrial DNA depletionAnnals of Neurology, 2004