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PISD is a mitochondrial disease gene causing skeletal dysplasia, cataracts, and white matter changes
Tian Zhao, Caitlin M. Goedhart, Pingdewinde Sam, Susanne Lingrell, Adam J. Cornish, Ryan E Lamont, Francois P Bernier, David Sinasac, Jillian S Parboosingh, Care4Rare Canada Consortium, Jean E. Vance, Steven M. Claypool, A Micheil Innes, Timothy E Shutt
doi: https://doi.org/10.1101/413070
Tian Zhao
1Alberta Children’s Hospital Research Institute, Department of Medical Genetics, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada
2Department of Biochemistry & Molecular Biology, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada
Caitlin M. Goedhart
1Alberta Children’s Hospital Research Institute, Department of Medical Genetics, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada
Pingdewinde Sam
3Department of Physiology, The Johns Hopkins University School of Medicine, Baltimore, MD, USA
Susanne Lingrell
4Dept of Medicine and Group on Molecular and Cell Biology of Lipids, University of Alberta, Edmonton, Alberta, Canada
Adam J. Cornish
3Department of Physiology, The Johns Hopkins University School of Medicine, Baltimore, MD, USA
Ryan E Lamont
1Alberta Children’s Hospital Research Institute, Department of Medical Genetics, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada
Francois P Bernier
1Alberta Children’s Hospital Research Institute, Department of Medical Genetics, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada
David Sinasac
1Alberta Children’s Hospital Research Institute, Department of Medical Genetics, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada
Jillian S Parboosingh
1Alberta Children’s Hospital Research Institute, Department of Medical Genetics, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada
Jean E. Vance
4Dept of Medicine and Group on Molecular and Cell Biology of Lipids, University of Alberta, Edmonton, Alberta, Canada
Steven M. Claypool
3Department of Physiology, The Johns Hopkins University School of Medicine, Baltimore, MD, USA
A Micheil Innes
1Alberta Children’s Hospital Research Institute, Department of Medical Genetics, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada
Timothy E Shutt
1Alberta Children’s Hospital Research Institute, Department of Medical Genetics, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada
2Department of Biochemistry & Molecular Biology, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada
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Posted September 12, 2018.
PISD is a mitochondrial disease gene causing skeletal dysplasia, cataracts, and white matter changes
Tian Zhao, Caitlin M. Goedhart, Pingdewinde Sam, Susanne Lingrell, Adam J. Cornish, Ryan E Lamont, Francois P Bernier, David Sinasac, Jillian S Parboosingh, Care4Rare Canada Consortium, Jean E. Vance, Steven M. Claypool, A Micheil Innes, Timothy E Shutt
bioRxiv 413070; doi: https://doi.org/10.1101/413070
PISD is a mitochondrial disease gene causing skeletal dysplasia, cataracts, and white matter changes
Tian Zhao, Caitlin M. Goedhart, Pingdewinde Sam, Susanne Lingrell, Adam J. Cornish, Ryan E Lamont, Francois P Bernier, David Sinasac, Jillian S Parboosingh, Care4Rare Canada Consortium, Jean E. Vance, Steven M. Claypool, A Micheil Innes, Timothy E Shutt
bioRxiv 413070; doi: https://doi.org/10.1101/413070
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