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Identification and description of three families with familial Alzheimer disease that segregate variants in the SORL1 gene.
Thonberg, Håkan; Chiang, Huei-Hsin; Lilius, Lena; Forsell, Charlotte; Lindström, Anna-Karin; Johansson, Charlotte; Björkström, Jenny; Thordardottir, Steinunn; Sleegers, Kristel; Van Broeckhoven, Christine; Rönnbäck, Annica; Graff, Caroline.
  • Thonberg H; Department NVS, Center for Alzheimer Research, Division for Neurogeriatrics, Karolinska Institutet, Huddinge, Sweden. hakan.thonberg@sll.se.
  • Chiang HH; Department of Geriatric Medicine, Genetics unit, Karolinska University Hospital, Stockholm, Sweden. hakan.thonberg@sll.se.
  • Lilius L; Department NVS, Center for Alzheimer Research, Division for Neurogeriatrics, Karolinska Institutet, Huddinge, Sweden.
  • Forsell C; Department of Geriatric Medicine, Genetics unit, Karolinska University Hospital, Stockholm, Sweden.
  • Lindström AK; Department NVS, Center for Alzheimer Research, Division for Neurogeriatrics, Karolinska Institutet, Huddinge, Sweden.
  • Johansson C; Department of Geriatric Medicine, Genetics unit, Karolinska University Hospital, Stockholm, Sweden.
  • Björkström J; Department NVS, Center for Alzheimer Research, Division for Neurogeriatrics, Karolinska Institutet, Huddinge, Sweden.
  • Thordardottir S; Department of Geriatric Medicine, Genetics unit, Karolinska University Hospital, Stockholm, Sweden.
  • Sleegers K; Department NVS, Center for Alzheimer Research, Division for Neurogeriatrics, Karolinska Institutet, Huddinge, Sweden.
  • Van Broeckhoven C; Department of Geriatric Medicine, Genetics unit, Karolinska University Hospital, Stockholm, Sweden.
  • Rönnbäck A; Department NVS, Center for Alzheimer Research, Division for Neurogeriatrics, Karolinska Institutet, Huddinge, Sweden.
  • Graff C; Department of Geriatric Medicine, Genetics unit, Karolinska University Hospital, Stockholm, Sweden.
Acta Neuropathol Commun ; 5(1): 43, 2017 06 09.
Article en En | MEDLINE | ID: mdl-28595629
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Proteínas de Transporte de Membrana / Variación Genética / Predisposición Genética a la Enfermedad / Proteínas Relacionadas con Receptor de LDL / Enfermedad de Alzheimer Tipo de estudio: Diagnostic_studies / Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Año: 2017 Tipo del documento: Article
Texto completo
Imprimir
XML
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Proteínas de Transporte de Membrana / Variación Genética / Predisposición Genética a la Enfermedad / Proteínas Relacionadas con Receptor de LDL / Enfermedad de Alzheimer Tipo de estudio: Diagnostic_studies / Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Año: 2017 Tipo del documento: Article