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Assessing non-Mendelian inheritance in inherited axonopathies.
Bis-Brewer, Dana M; Gan-Or, Ziv; Sleiman, Patrick; Hakonarson, Hakon; Fazal, Sarah; Courel, Steve; Cintra, Vivian; Tao, Feifei; Estiar, Mehrdad A; Tarnopolsky, Mark; Boycott, Kym M; Yoon, Grace; Suchowersky, Oksana; Dupré, Nicolas; Cheng, Andrew; Lloyd, Thomas E; Rouleau, Guy; Schüle, Rebecca; Züchner, Stephan.
Afiliação
  • Bis-Brewer DM; Dr. John T. Macdonald Foundation Department of Human Genetics, John P. Hussman Institute for Human Genomics, University of Miami Miller School of Medicine, Miami, FL, USA. dmb107@miami.edu.
  • Gan-Or Z; Department of Human Genetics, McGill University, Montréal, QC, Canada.
  • Sleiman P; Montreal Neurological Institute and Hospital, McGill University, Montréal, QC, Canada.
  • Hakonarson H; Center for Applied Genomics, The Children's Hospital of Philadelphia; Division of Human Genetics, Department of Pediatrics, The Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
  • Courel S; Center for Applied Genomics, The Children's Hospital of Philadelphia; Division of Human Genetics, Department of Pediatrics, The Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
  • Cintra V; Dr. John T. Macdonald Foundation Department of Human Genetics, John P. Hussman Institute for Human Genomics, University of Miami Miller School of Medicine, Miami, FL, USA.
  • Tao F; Dr. John T. Macdonald Foundation Department of Human Genetics, John P. Hussman Institute for Human Genomics, University of Miami Miller School of Medicine, Miami, FL, USA.
  • Estiar MA; Dr. John T. Macdonald Foundation Department of Human Genetics, John P. Hussman Institute for Human Genomics, University of Miami Miller School of Medicine, Miami, FL, USA.
  • Tarnopolsky M; Dr. John T. Macdonald Foundation Department of Human Genetics, John P. Hussman Institute for Human Genomics, University of Miami Miller School of Medicine, Miami, FL, USA.
  • Boycott KM; Department of Human Genetics, McGill University, Montréal, QC, Canada.
  • Yoon G; Montreal Neurological Institute and Hospital, McGill University, Montréal, QC, Canada.
  • Suchowersky O; Neuromuscular and Neurometabolics Division, Department of Pediatrics, McMaster University, Hamilton, ON, Canada.
  • Dupré N; Children's Hospital of Eastern Ontario Research Institute, University of Ottawa, Ottawa, ON, Canada.
  • Cheng A; Division of Clinical and Metabolic Genetics, Department of Paediatrics, The Hospital for Sick Children, University of Toronto, Toronto, ON, Canada.
  • Lloyd TE; Division of Neurology, Department of Paediatrics, The Hospital for Sick Children, University of Toronto, Toronto, ON, Canada.
  • Rouleau G; Department of Medicine, Medical Genetics and Pediatrics, University of Alberta, Edmonton, AB, Canada.
  • Schüle R; Division of Neurosciences, CHU de Québec, Université Laval, Québec City, QC, Canada.
  • Züchner S; Department of Medicine, Faculty of Medicine, Université Laval, Québec City, QC, Canada.
Genet Med ; 22(12): 2114-2119, 2020 12.
Article em En | MEDLINE | ID: mdl-32741968
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Paraplegia Espástica Hereditária / Doença de Charcot-Marie-Tooth Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2020 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Paraplegia Espástica Hereditária / Doença de Charcot-Marie-Tooth Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2020 Tipo de documento: Article