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The wide genetic landscape of clinical frontotemporal dementia: systematic combined sequencing of 121 consecutive subjects.
Blauwendraat, Cornelis; Wilke, Carlo; Simón-Sánchez, Javier; Jansen, Iris E; Reifschneider, Anika; Capell, Anja; Haass, Christian; Castillo-Lizardo, Melissa; Biskup, Saskia; Maetzler, Walter; Rizzu, Patrizia; Heutink, Peter; Synofzik, Matthis.
Afiliação
  • Blauwendraat C; Applied Genomics for Neurodegenerative Diseases, German Center for Neurodegenerative Diseases (DZNE), Tübingen, Germany.
  • Wilke C; Department of Neurodegenerative Diseases, Hertie Institute for Clinical Brain Research, University of Tübingen, Tübingen Germany.
  • Simón-Sánchez J; Neurodegeneration, German Center for Neurodegenerative Diseases (DZNE), Tübingen, Germany.
  • Jansen IE; Department of Neurodegenerative Diseases, Hertie Institute for Clinical Brain Research, University of Tübingen, Tübingen Germany.
  • Reifschneider A; Neurodegeneration, German Center for Neurodegenerative Diseases (DZNE), Tübingen, Germany.
  • Capell A; Genome Biology of Neurodegenerative Diseases, German Center for Neurodegenerative Diseases (DZNE), Tübingen, Germany.
  • Haass C; Biomedical Center (BMC), Biochemistry, Ludwig-Maximilians-Universität München, Munich, Germany.
  • Castillo-Lizardo M; Biomedical Center (BMC), Biochemistry, Ludwig-Maximilians-Universität München, Munich, Germany.
  • Biskup S; Biomedical Center (BMC), Biochemistry, Ludwig-Maximilians-Universität München, Munich, Germany.
  • Maetzler W; Munich Cluster for Systems Neurology (SyNergy), Munich, Germany.
  • Rizzu P; German Center for Neurodegenerative Diseases (DZNE) Munich, Munich, Germany.
  • Heutink P; Applied Genomics for Neurodegenerative Diseases, German Center for Neurodegenerative Diseases (DZNE), Tübingen, Germany.
  • Synofzik M; Center for Genomics and Transcriptomics, Tübingen, Germany.
Genet Med ; 20(2): 240-249, 2018 02.
Article em En | MEDLINE | ID: mdl-28749476
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Predisposição Genética para Doença / Demência Frontotemporal / Estudos de Associação Genética Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Female / Humans / Male / Middle aged Idioma: En Revista: Genet Med Ano de publicação: 2018 Tipo de documento: Article
Texto completo
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Predisposição Genética para Doença / Demência Frontotemporal / Estudos de Associação Genética Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Female / Humans / Male / Middle aged Idioma: En Revista: Genet Med Ano de publicação: 2018 Tipo de documento: Article