Your browser doesn't support javascript.
loading
Multi-infarct dementia of Swedish type is caused by a 3'UTR mutation of COL4A1.
Siitonen, Maija; Börjesson-Hanson, Anne; Pöyhönen, Minna; Ora, Ari; Pasanen, Petra; Bras, Jose; Kern, Silke; Kern, Jürgen; Andersen, Oluf; Stanescu, Horia; Kleta, Robert; Baumann, Marc; Kalaria, Rajesh; Kalimo, Hannu; Singleton, Andy; Hardy, John; Viitanen, Matti; Myllykangas, Liisa; Guerreiro, Rita.
Afiliación
  • Siitonen M; Department of Medical Biochemistry and Genetics, University of Turku, Turku, Finland.
  • Börjesson-Hanson A; Department of Psychiatry and Neurochemistry, Institute of Neuroscience and Physiology, Sahlgrenska Academy at the University of Gothenburg, Gothenburg, Sweden.
  • Pöyhönen M; Department of Clinical Genetics, Helsinki University Central Hospital, Helsinki, Finland.
  • Ora A; Department of Medical and Clinical Genetics, University of Helsinki, Helsinki, Finland.
  • Pasanen P; Department of Applied Physics, Aalto University, Espoo, Finland.
  • Bras J; Department of Medical Biochemistry and Genetics, University of Turku, Turku, Finland.
  • Kern S; Tyks Microbiology and Genetics, Turku University Hospital, Turku, Finland.
  • Kern J; Department of Molecular Neuroscience, Institute of Neurology, University College London, London, UK.
  • Andersen O; Department of Medical Sciences and Institute of Biomedicine - iBiMED, University of Aveiro, Aveiro, Portugal.
  • Stanescu H; Department of Psychiatry and Neurochemistry, Institute of Neuroscience and Physiology, Sahlgrenska Academy at the University of Gothenburg, Gothenburg, Sweden.
  • Kleta R; Department of Psychiatry and Neurochemistry, Institute of Neuroscience and Physiology, Sahlgrenska Academy at the University of Gothenburg, Gothenburg, Sweden.
  • Baumann M; Department of Clinical Neuroscience, Institute of Neuroscience and Physiology, Sahlgrenska Academy at the University of Gothenburg, Gothenburg, Sweden.
  • Kalaria R; Centre for Nephrology University College London, London, UK.
  • Kalimo H; Centre for Nephrology University College London, London, UK.
  • Singleton A; Meilahti Clinical Proteomics Core Unit, Department of Biochemistry and Developmental Biology, Biomedicum Helsinki, University of Helsinki, Helsinki, Finland.
  • Hardy J; Institute of Neuroscience, Newcastle University, Campus for Ageing and Vitality, Newcastle upon Tyne, UK.
  • Viitanen M; Department of Pathology, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.
  • Myllykangas L; Laboratory of Neurogenetics, National Institute on Aging, Bethesda, MD, USA.
  • Guerreiro R; Department of Molecular Neuroscience, Institute of Neurology, University College London, London, UK.
Brain ; 140(5): e29, 2017 05 01.
Article en En | MEDLINE | ID: mdl-28369186
Asunto(s)
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Demencia por Múltiples Infartos / Salud de la Familia / Predisposición Genética a la Enfermedad / Regiones no Traducidas 3' / Colágeno Tipo IV / Mutación Límite: Female / Humans / Male País/Región como asunto: Europa Idioma: En Revista: Brain Año: 2017 Tipo del documento: Article País de afiliación: Finlandia
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Demencia por Múltiples Infartos / Salud de la Familia / Predisposición Genética a la Enfermedad / Regiones no Traducidas 3' / Colágeno Tipo IV / Mutación Límite: Female / Humans / Male País/Región como asunto: Europa Idioma: En Revista: Brain Año: 2017 Tipo del documento: Article País de afiliación: Finlandia