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MITO-FIND: A study in 390 patients to determine a diagnostic strategy for mitochondrial disease.
Kerr, Marina; Hume, Stacey; Omar, Fadya; Koo, Desmond; Barnes, Heather; Khan, Maida; Aman, Suhaib; Wei, Xing-Chang; Alfuhaid, Hanen; McDonald, Roman; McDonald, Liam; Newell, Christopher; Sparkes, Rebecca; Hittel, Dustin; Khan, Aneal.
Afiliación
  • Kerr M; Departments of Medical Genetics and Pediatrics, University of Calgary Cumming School of Medicine, Alberta Children's Hospital Research Institute, Calgary, Alberta, Canada.
  • Hume S; Department of Medical Genetics, University of Alberta, Edmonton, Canada.
  • Omar F; Departments of Medical Genetics and Pediatrics, University of Calgary Cumming School of Medicine, Alberta Children's Hospital Research Institute, Calgary, Alberta, Canada.
  • Koo D; Departments of Medical Genetics and Pediatrics, University of Calgary Cumming School of Medicine, Alberta Children's Hospital Research Institute, Calgary, Alberta, Canada.
  • Barnes H; Departments of Medical Genetics and Pediatrics, University of Calgary Cumming School of Medicine, Alberta Children's Hospital Research Institute, Calgary, Alberta, Canada.
  • Khan M; Departments of Medical Genetics and Pediatrics, University of Calgary Cumming School of Medicine, Alberta Children's Hospital Research Institute, Calgary, Alberta, Canada.
  • Aman S; Departments of Medical Genetics and Pediatrics, University of Calgary Cumming School of Medicine, Alberta Children's Hospital Research Institute, Calgary, Alberta, Canada.
  • Wei XC; Department of Radiology, Alberta Children's Hospital, University of Calgary Cumming School of Medicine, Calgary, Alberta, Canada.
  • Alfuhaid H; Departments of Medical Genetics and Pediatrics, University of Calgary Cumming School of Medicine, Alberta Children's Hospital Research Institute, Calgary, Alberta, Canada.
  • McDonald R; Departments of Medical Genetics and Pediatrics, University of Calgary Cumming School of Medicine, Alberta Children's Hospital Research Institute, Calgary, Alberta, Canada.
  • McDonald L; Departments of Medical Genetics and Pediatrics, University of Calgary Cumming School of Medicine, Alberta Children's Hospital Research Institute, Calgary, Alberta, Canada.
  • Newell C; Departments of Medical Genetics and Pediatrics, University of Calgary Cumming School of Medicine, Alberta Children's Hospital Research Institute, Calgary, Alberta, Canada.
  • Sparkes R; Departments of Medical Genetics and Pediatrics, University of Calgary Cumming School of Medicine, Alberta Children's Hospital Research Institute, Calgary, Alberta, Canada.
  • Hittel D; Department of Biochemistry & Molecular Biology, Cumming School of Medicine, University of Calgary, Calgary, AB, Canada.
  • Khan A; Departments of Medical Genetics and Pediatrics, University of Calgary Cumming School of Medicine, Alberta Children's Hospital Research Institute, Calgary, Alberta, Canada. Electronic address: khaa@ucalgary.ca.
Mol Genet Metab ; 131(1-2): 66-82, 2020.
Article en En | MEDLINE | ID: mdl-32980267
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: ADN Mitocondrial / Enfermedades Mitocondriales / Mitocondrias Tipo de estudio: Diagnostic_studies Límite: Adult / Child / Child, preschool / Female / Humans / Male / Middle aged Idioma: En Revista: Mol Genet Metab Asunto de la revista: BIOLOGIA MOLECULAR / BIOQUIMICA / METABOLISMO Año: 2020 Tipo del documento: Article País de afiliación: Canadá
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: ADN Mitocondrial / Enfermedades Mitocondriales / Mitocondrias Tipo de estudio: Diagnostic_studies Límite: Adult / Child / Child, preschool / Female / Humans / Male / Middle aged Idioma: En Revista: Mol Genet Metab Asunto de la revista: BIOLOGIA MOLECULAR / BIOQUIMICA / METABOLISMO Año: 2020 Tipo del documento: Article País de afiliación: Canadá