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17q21.31 duplication causes prominent tau-related dementia with increased MAPT expression.
Le Guennec, K; Quenez, O; Nicolas, G; Wallon, D; Rousseau, S; Richard, A-C; Alexander, J; Paschou, P; Charbonnier, C; Bellenguez, C; Grenier-Boley, B; Lechner, D; Bihoreau, M-T; Olaso, R; Boland, A; Meyer, V; Deleuze, J-F; Amouyel, P; Munter, H M; Bourque, G; Lathrop, M; Frebourg, T; Redon, R; Letenneur, L; Dartigues, J-F; Martinaud, O; Kalev, O; Mehrabian, S; Traykov, L; Ströbel, T; Le Ber, I; Caroppo, P; Epelbaum, S; Jonveaux, T; Pasquier, F; Rollin-Sillaire, A; Génin, E; Guyant-Maréchal, L; Kovacs, G G; Lambert, J-C; Hannequin, D; Campion, D; Rovelet-Lecrux, A.
Afiliação
  • Le Guennec K; Inserm, U1079, faculté de médecine, Rouen University, IRIB, Normandy University, Rouen, France.
  • Quenez O; Normandy Centre for Genomic Medicine and Personalized Medicine, Rouen, France.
  • Nicolas G; Inserm, U1079, faculté de médecine, Rouen University, IRIB, Normandy University, Rouen, France.
  • Wallon D; Normandy Centre for Genomic Medicine and Personalized Medicine, Rouen, France.
  • Rousseau S; CNR-MAJ, Rouen University Hospital, Rouen, France.
  • Richard AC; Inserm, U1079, faculté de médecine, Rouen University, IRIB, Normandy University, Rouen, France.
  • Alexander J; Normandy Centre for Genomic Medicine and Personalized Medicine, Rouen, France.
  • Paschou P; CNR-MAJ, Rouen University Hospital, Rouen, France.
  • Charbonnier C; Department of Genetics, Rouen University Hospital, Rouen, France.
  • Bellenguez C; Inserm, U1079, faculté de médecine, Rouen University, IRIB, Normandy University, Rouen, France.
  • Grenier-Boley B; Normandy Centre for Genomic Medicine and Personalized Medicine, Rouen, France.
  • Lechner D; CNR-MAJ, Rouen University Hospital, Rouen, France.
  • Bihoreau MT; Department of Neurology, Rouen University Hospital, Rouen, France.
  • Olaso R; Inserm, U1079, faculté de médecine, Rouen University, IRIB, Normandy University, Rouen, France.
  • Boland A; Normandy Centre for Genomic Medicine and Personalized Medicine, Rouen, France.
  • Meyer V; CNR-MAJ, Rouen University Hospital, Rouen, France.
  • Deleuze JF; Inserm, U1079, faculté de médecine, Rouen University, IRIB, Normandy University, Rouen, France.
  • Amouyel P; Normandy Centre for Genomic Medicine and Personalized Medicine, Rouen, France.
  • Munter HM; CNR-MAJ, Rouen University Hospital, Rouen, France.
  • Bourque G; Department of Molecular Biology and Genetics, Democritus University of Thrace, Alexandroupoli, Greece.
  • Lathrop M; Department of Molecular Biology and Genetics, Democritus University of Thrace, Alexandroupoli, Greece.
  • Frebourg T; Inserm, U1079, faculté de médecine, Rouen University, IRIB, Normandy University, Rouen, France.
  • Redon R; Normandy Centre for Genomic Medicine and Personalized Medicine, Rouen, France.
  • Letenneur L; CNR-MAJ, Rouen University Hospital, Rouen, France.
  • Dartigues JF; Inserm, U1167, Lille, France.
  • Martinaud O; Institut Pasteur de Lille, Lille, France.
  • Kalev O; Université Lille-Nord de France, Lille, France.
  • Mehrabian S; Inserm, U1167, Lille, France.
  • Traykov L; Institut Pasteur de Lille, Lille, France.
  • Ströbel T; Université Lille-Nord de France, Lille, France.
  • Le Ber I; Centre National de Génotypage, Institut de Génomique, CEA, Evry, France.
  • Caroppo P; Centre National de Génotypage, Institut de Génomique, CEA, Evry, France.
  • Epelbaum S; Centre National de Génotypage, Institut de Génomique, CEA, Evry, France.
  • Jonveaux T; Centre National de Génotypage, Institut de Génomique, CEA, Evry, France.
  • Pasquier F; Centre National de Génotypage, Institut de Génomique, CEA, Evry, France.
  • Rollin-Sillaire A; Centre National de Génotypage, Institut de Génomique, CEA, Evry, France.
  • Génin E; Fondation Jean Dausset, Centre d'études du Polymorphisme Humain, Paris, France.
  • Guyant-Maréchal L; Inserm, U1167, Lille, France.
  • Kovacs GG; Institut Pasteur de Lille, Lille, France.
  • Lambert JC; Université Lille-Nord de France, Lille, France.
  • Hannequin D; McGill University and Génome Québec Innovation Centre, Montréal, QC, Canada.
  • Campion D; McGill University and Génome Québec Innovation Centre, Montréal, QC, Canada.
  • Rovelet-Lecrux A; McGill University and Génome Québec Innovation Centre, Montréal, QC, Canada.
Mol Psychiatry ; 22(8): 1119-1125, 2017 08.
Article em En | MEDLINE | ID: mdl-27956742
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Cromossomos Humanos Par 17 / Demência / Doença de Alzheimer Tipo de estudo: Etiology_studies / Observational_studies Limite: Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2017 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Cromossomos Humanos Par 17 / Demência / Doença de Alzheimer Tipo de estudo: Etiology_studies / Observational_studies Limite: Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2017 Tipo de documento: Article