POLG mutations associated with Alpers' syndrome and mitochondrial DNA depletion
Version of Record online: 30 MAR 2004
Copyright © 2003 American Neurological Association
Annals of Neurology
Volume 55, Issue 5, pages 706–712, May 2004
How to Cite
Naviaux, R. K. and Nguyen, K. V. (2004), POLG mutations associated with Alpers' syndrome and mitochondrial DNA depletion. Ann Neurol., 55: 706–712. doi: 10.1002/ana.20079
- Issue online: 21 APR 2004
- Version of Record online: 30 MAR 2004
- Manuscript Accepted: 4 FEB 2004
- Manuscript Revised: 9 JAN 2004
- Manuscript Received: 24 SEP 2003
- Edward Mallinckrodt
- Jr. Foundation
- The UCSD Foundation Christini Fund
- The David Campbell Foundation
- The San Diego Medical Education and Research Foundation
- The Tyler Riff Ferguson Medical Research Foundation
- The People of Cumberland Maryland and the Tri-State Area
- The Scott Pawlowski Mitochondrial Research Fund
- National Institutes of Health grant to the UCSD General Clinical Research Center. Grant Number: MOI RR00827
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