Your browser doesn't support javascript.
loading
Somatic variants in autosomal dominant genes are a rare cause of sporadic Alzheimer's disease.
Nicolas, Gaël; Acuña-Hidalgo, Rocío; Keogh, Michael J; Quenez, Olivier; Steehouwer, Marloes; Lelieveld, Stefan; Rousseau, Stéphane; Richard, Anne-Claire; Oud, Manon S; Marguet, Florent; Laquerrière, Annie; Morris, Chris M; Attems, Johannes; Smith, Colin; Ansorge, Olaf; Al Sarraj, Safa; Frebourg, Thierry; Campion, Dominique; Hannequin, Didier; Wallon, David; Gilissen, Christian; Chinnery, Patrick F; Veltman, Joris A; Hoischen, Alexander.
Afiliación
  • Nicolas G; Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands; Normandie Univ, UNIROUEN, Inserm U1245 and Rouen University Hospital, Department of Genetics and CNR-MAJ, F 76000, Normandy Center for Genomic and Personalized Medicine, Rouen, France. Electronic address: gae
  • Acuña-Hidalgo R; Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands; Max Planck Institute for Molecular Genetics, RG Development & Disease, Berlin, Germany.
  • Keogh MJ; Department of Clinical Neurosciences, University of Cambridge, Cambridge Biomedical Campus, Cambridge, CB2 0QQ, UK; MRC Mitochondrial Biology Unit, University of Cambridge, Cambridge, CB2 0XY, UK.
  • Quenez O; Normandie Univ, UNIROUEN, Inserm U1245 and Rouen University Hospital, Department of Genetics and CNR-MAJ, F 76000, Normandy Center for Genomic and Personalized Medicine, Rouen, France.
  • Steehouwer M; Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands.
  • Lelieveld S; Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands.
  • Rousseau S; Normandie Univ, UNIROUEN, Inserm U1245 and Rouen University Hospital, Department of Genetics and CNR-MAJ, F 76000, Normandy Center for Genomic and Personalized Medicine, Rouen, France.
  • Richard AC; Normandie Univ, UNIROUEN, Inserm U1245 and Rouen University Hospital, Department of Genetics and CNR-MAJ, F 76000, Normandy Center for Genomic and Personalized Medicine, Rouen, France.
  • Oud MS; Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands.
  • Marguet F; Normandie Univ, UNIROUEN, Inserm U1245 and Rouen University Hospital, Department of Neuropathology, F 76000, Normandy Center for Genomic and Personalized Medicine, Rouen, France.
  • Laquerrière A; Normandie Univ, UNIROUEN, Inserm U1245 and Rouen University Hospital, Department of Neuropathology, F 76000, Normandy Center for Genomic and Personalized Medicine, Rouen, France.
  • Morris CM; Institute of Neuroscience, Newcastle University, Newcastle Upon Tyne, NE4 5PL, UK.
  • Attems J; Institute of Neuroscience, Newcastle University, Newcastle Upon Tyne, NE4 5PL, UK.
  • Smith C; National CJD Research & Surveillance Unit, Centre for Clinical Brain Sciences, University of Edinburgh, Western General Hospital, Edinburgh, EH4 2XU, UK.
  • Ansorge O; Department of Neuropathology, John Radcliffe Hospital, Oxford, OX3 9DU, UK.
  • Al Sarraj S; Department of Basic and Clinical Neuroscience, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, SE5 8AF, UK.
  • Frebourg T; Normandie Univ, UNIROUEN, Inserm U1245 and Rouen University Hospital, Department of Genetics and CNR-MAJ, F 76000, Normandy Center for Genomic and Personalized Medicine, Rouen, France.
  • Campion D; Normandie Univ, UNIROUEN, Inserm U1245 and Rouen University Hospital, Department of Genetics and CNR-MAJ, F 76000, Normandy Center for Genomic and Personalized Medicine, Rouen, France; Department of research, Rouvray Psychiatric Hospital, Sotteville-lès-Rouen, France.
  • Hannequin D; Normandie Univ, UNIROUEN, Inserm U1245 and Rouen University Hospital, Department of Genetics, Department of Neurology and CNR-MAJ, F 76000, Normandy Center for Genomic and Personalized Medicine, Rouen, France.
  • Wallon D; Normandie Univ, UNIROUEN, Inserm U1245 and Rouen University Hospital, Department of Neurology and CNR-MAJ, F 76000, Normandy Center for Genomic and Personalized Medicine, Rouen, France.
  • Gilissen C; Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands.
  • Chinnery PF; Department of Clinical Neurosciences, University of Cambridge, Cambridge Biomedical Campus, Cambridge, CB2 0QQ, UK; MRC Mitochondrial Biology Unit, University of Cambridge, Cambridge, CB2 0XY, UK.
  • Veltman JA; Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands; Institute of Genetic Medicine, International Centre for Life, Newcastle University, Newcastle upon Tyne, United Kingdom.
  • Hoischen A; Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands; Department of Internal Medicine and Radboud Center for Infectious Diseases (RCI), Radboud University Medical Center, Nijmegen, The Netherlands.
Alzheimers Dement ; 14(12): 1632-1639, 2018 12.
Article en En | MEDLINE | ID: mdl-30114415
Asunto(s)
Palabras clave
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Predisposición Genética a la Enfermedad / Enfermedad de Alzheimer Límite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Alzheimers Dement Año: 2018 Tipo del documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Predisposición Genética a la Enfermedad / Enfermedad de Alzheimer Límite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Alzheimers Dement Año: 2018 Tipo del documento: Article