A Method for Next-Generation Sequencing of Paired Diagnostic and Remission Samples to Detect Mitochondrial DNA Mutations Associated with Leukemia

The Journal of Molecular Diagnostics - Tập 19 - Trang 711-721 - 2017
Ilaria S. Pagani1, Chung H. Kok1,2, Verity A. Saunders1, Mark B. Van der Hoek1, Susan L. Heatley1,2, Anthony P. Schwarer3,4, Christopher N. Hahn2,5, Timothy P. Hughes1,2,3,5,6, Deborah L. White1,2,3,7, David M. Ross1,2,3,6,8
1Cancer Theme, South Australian Health and Medical Research Institute, Adelaide, South Australia, Australia
2School of Medicine, Faculty of Health Sciences, University of Adelaide, Adelaide, South Australia, Australia
3Australasian Leukaemia and Lymphoma Group, Melbourne, Victoria, Australia
4Department of Haematology, Box Hill Hospital, Melbourne, Victoria, Australia
5Centre for Cancer Biology, SA Pathology, Adelaide, South Australia, Australia
6Department of Haematology, Royal Adelaide Hospital and SA Pathology, Adelaide, South Australia, Australia
7School of Biomedical Sciences, Faculty of Sciences, University of Adelaide, Adelaide, South Australia, Australia
8Department of Molecular Medicine and Pathology, Flinders University and Medical Centre, Adelaide, South Australia, Australia

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