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Open Access
Peer-reviewed
Research Article
Whole-genome sequencing suggests mechanisms for 22q11.2 deletion-associated Parkinson’s disease
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Nancy J. Butcher,
Current address: Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, United States of America
Affiliations Clinical Genetics Research Program, Centre for Addiction and Mental Health, Toronto, Ontario, Canada, Campbell Family Mental Health Research Institute, Centre for Addiction and Mental Health, Toronto, Ontario, Canada, Institute of Medical Science, University of Toronto, Toronto, Ontario, Canada
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Daniele Merico,
Affiliation The Centre for Applied Genomics and Program in Genetics and Genome Biology, The Hospital for Sick Children, Toronto, Ontario, Canada
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Mehdi Zarrei,
Affiliation The Centre for Applied Genomics and Program in Genetics and Genome Biology, The Hospital for Sick Children, Toronto, Ontario, Canada
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Lucas Ogura,
Affiliation Clinical Genetics Research Program, Centre for Addiction and Mental Health, Toronto, Ontario, Canada
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Christian R. Marshall,
Affiliations The Centre for Applied Genomics and Program in Genetics and Genome Biology, The Hospital for Sick Children, Toronto, Ontario, Canada, McLaughlin Centre and Department of Molecular Genetics, University of Toronto, Toronto, Ontario, Canada
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Eva W. C. Chow,
Affiliations Clinical Genetics Research Program, Centre for Addiction and Mental Health, Toronto, Ontario, Canada, Campbell Family Mental Health Research Institute, Centre for Addiction and Mental Health, Toronto, Ontario, Canada, Department of Psychiatry, University of Toronto, Toronto, Ontario, Canada
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Anthony E. Lang,
Affiliations Institute of Medical Science, University of Toronto, Toronto, Ontario, Canada, Division of Neurology, Department of Medicine, University of Toronto, Toronto, Ontario, Canada, Tanz Centre for Research in Neurodegenerative Diseases, Department of Medicine, University of Toronto, Toronto, Ontario, Canada, Toronto Western Hospital Research Institute, University Health Network, Toronto, Ontario, Canada, Edmond J. Safra Program in Parkinson’s Disease, Toronto Western Hospital, Toronto, Ontario, Canada
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Stephen W. Scherer,
Affiliations Institute of Medical Science, University of Toronto, Toronto, Ontario, Canada, The Centre for Applied Genomics and Program in Genetics and Genome Biology, The Hospital for Sick Children, Toronto, Ontario, Canada, McLaughlin Centre and Department of Molecular Genetics, University of Toronto, Toronto, Ontario, Canada
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Anne S. Bassett
* E-mail: anne.bassett@utoronto.ca
Affiliations Clinical Genetics Research Program, Centre for Addiction and Mental Health, Toronto, Ontario, Canada, Campbell Family Mental Health Research Institute, Centre for Addiction and Mental Health, Toronto, Ontario, Canada, Institute of Medical Science, University of Toronto, Toronto, Ontario, Canada, Department of Psychiatry, University of Toronto, Toronto, Ontario, Canada, Toronto General Research Institute, University Health Network, Toronto, Ontario, Canada, The Dalglish 22q Clinic for Adults with 22q11.2 Deletion Syndrome, University Health Network, Toronto, Ontario, Canada, Department of Psychiatry, University Health Network, Toronto, Ontario, Canada, Division of Cardiology, Department of Medicine, University Health Network, Toronto, Ontario, Canada
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Whole-genome sequencing suggests mechanisms for 22q11.2 deletion-associated Parkinson’s disease
- Nancy J. Butcher,
- Daniele Merico,
- Mehdi Zarrei,
- Lucas Ogura,
- Christian R. Marshall,
- Eva W. C. Chow,
- Anthony E. Lang,
- Stephen W. Scherer,
- Anne S. Bassett
- Published: April 21, 2017
- https://doi.org/10.1371/journal.pone.0173944