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Common variation near IRF6 is associated with IFN-ß-induced liver injury in multiple sclerosis.
Kowalec, Kaarina; Wright, Galen E B; Drögemöller, Britt I; Aminkeng, Folefac; Bhavsar, Amit P; Kingwell, Elaine; Yoshida, Eric M; Traboulsee, Anthony; Marrie, Ruth Ann; Kremenchutzky, Marcelo; Campbell, Trudy L; Duquette, Pierre; Chalasani, Naga; Wadelius, Mia; Hallberg, Pär; Xia, Zongqi; De Jager, Philip L; Denny, Joshua C; Davis, Mary F; Ross, Colin J D; Tremlett, Helen; Carleton, Bruce C.
Afiliación
  • Kowalec K; Division of Neurology, Faculty of Medicine, University of British Columbia, Vancouver, British Columbia, Canada.
  • Wright GEB; Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden.
  • Drögemöller BI; Division of Translational Therapeutics, Department of Pediatrics, University of British Columbia, Vancouver, British Columbia, Canada.
  • Aminkeng F; Division of Translational Therapeutics, Department of Pediatrics, University of British Columbia, Vancouver, British Columbia, Canada.
  • Bhavsar AP; British Columbia Children's Hospital Research Institute, Vancouver, British Columbia, Canada.
  • Kingwell E; Department of Medical Genetics, Faculty of Medicine, University of British Columbia, Vancouver, British Columbia, Canada.
  • Yoshida EM; Division of Translational Therapeutics, Department of Pediatrics, University of British Columbia, Vancouver, British Columbia, Canada.
  • Traboulsee A; British Columbia Children's Hospital Research Institute, Vancouver, British Columbia, Canada.
  • Marrie RA; Faculty of Pharmaceutical Sciences, University of British Columbia, Vancouver, British Columbia, Canada.
  • Kremenchutzky M; Department of Pharmacology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.
  • Campbell TL; Translational Laboratory in Genetic Medicine, Agency for Science, Technology and Research, Singapore, Singapore.
  • Duquette P; British Columbia Children's Hospital Research Institute, Vancouver, British Columbia, Canada.
  • Chalasani N; Faculty of Pharmaceutical Sciences, University of British Columbia, Vancouver, British Columbia, Canada.
  • Wadelius M; Department of Medical Microbiology and Immunology, Faculty of Medicine and Dentistry, University of Alberta, Edmonton, Alberta, Canada.
  • Hallberg P; Division of Neurology, Faculty of Medicine, University of British Columbia, Vancouver, British Columbia, Canada.
  • Xia Z; Division of Gastroenterology, Faculty of Medicine, University of British Columbia, Vancouver, British Columbia, Canada.
  • De Jager PL; Division of Neurology, Faculty of Medicine, University of British Columbia, Vancouver, British Columbia, Canada.
  • Denny JC; Department of Internal Medicine, Max Rady College of Medicine, Rady Faculty of Health Sciences, University of Manitoba, Winnipeg, Manitoba, Canada.
  • Davis MF; Department of Community Health Sciences, Max Rady College of Medicine, Rady Faculty of Health Sciences, University of Manitoba, Winnipeg, Manitoba, Canada.
  • Ross CJD; London Health Sciences Centre and Department of Clinical Neurological Sciences, Faculty of Medicine, Western University, London, Ontario, Canada.
  • Tremlett H; Dalhousie Multiple Sclerosis Research Unit and School of Nursing, Dalhousie University, Halifax, Nova Scotia, Canada.
  • Carleton BC; Department of Neurosciences, Université de Montréal, Montreal, Quebec, Canada.
Nat Genet ; 50(8): 1081-1085, 2018 08.
Article en En | MEDLINE | ID: mdl-30013178
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Variación Genética / Interferón beta / Factores Reguladores del Interferón / Enfermedad Hepática Inducida por Sustancias y Drogas / Esclerosis Múltiple Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Female / Humans / Male Idioma: En Revista: Nat Genet Asunto de la revista: GENETICA MEDICA Año: 2018 Tipo del documento: Article País de afiliación: Canadá
Texto completo
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Variación Genética / Interferón beta / Factores Reguladores del Interferón / Enfermedad Hepática Inducida por Sustancias y Drogas / Esclerosis Múltiple Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Female / Humans / Male Idioma: En Revista: Nat Genet Asunto de la revista: GENETICA MEDICA Año: 2018 Tipo del documento: Article País de afiliación: Canadá