Clinical and molecular features of mitochondrial DNA depletion due to mutations in deoxyguanosine kinase.

© 2007 WILEY-LISS, INC. Received 24 July 2007; accepted revised manuscript 24 September 2007. Clinical and Molecular Features of Mitochondrial DNA Depletion Due to Mutations in Deoxyguanosine Kinase D. P. Dimmock, Q. Zhang, C. Dionisi-Vici R. Carrozzo, J. Shieh, L-Y Tang, C. Truong, E. Schmitt, M. Sifry-Platt, , S. Lucioli, F.M. Santorelli, C. H. Ficicioglu, M Rodriguez, K. Wierenga, G. M. Enns, N. Longo, M. H. Lipson, H Vallance, W.J. Craigen, F Scaglia, and L-J. Wong* Molecular and Human Genetics, Baylor College of Medicine, Houston, TX; Division of Metabolism, Children’s Hospital “Bambino Gesu”, Rome, Italy; Unit of Molecular Medicine, Children’s Hospital “Bambino Gesu”, Rome, Italy; Medical Genetics, J. David Gladstone Institute at UCSF, San Francisco, CA; Department of Medical Genetics, Kaiser Permanente, Sacramento, CA; Section of Metabolism, Children's Hospital Philadelphia, Philadelphia, PA; Department of Pathology, Miller School of Medicine, University of Miami, Miami, FL; Dr. John T. Macdonald Foundation Center for Medical Genetics, Miller School of Medicine, University of Miami, Miami, FL; Division of Medical Genetics, Stanford University School of Medicine, Stanford, CA; Department of Pediatrics, Division of Medical Genetics, University of Utah, Salt Lake City, UT; Department of Pathology & Laboratory Medicine, University of British Columbia, Vancouver, B.C., Canada.