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A comprehensive analysis of copy number variation in a Turkish dementia cohort.
Dehghani, Nadia; Guven, Gamze; Kun-Rodrigues, Celia; Gouveia, Catarina; Foster, Kalina; Hanagasi, Hasmet; Lohmann, Ebba; Samanci, Bedia; Gurvit, Hakan; Bilgic, Basar; Bras, Jose; Guerreiro, Rita.
Afiliación
  • Dehghani N; Department of Neurodegenerative Science, Van Andel Institute, Grand Rapids, Michigan, USA.
  • Guven G; Department of Genetics, Aziz Sancar Institute of Experimental Medicine, Istanbul University, Istanbul, Turkey.
  • Kun-Rodrigues C; Department of Neurodegenerative Science, Van Andel Institute, Grand Rapids, Michigan, USA.
  • Gouveia C; Department of Neurodegenerative Science, Van Andel Institute, Grand Rapids, Michigan, USA.
  • Foster K; Department of Neurodegenerative Science, Van Andel Institute, Grand Rapids, Michigan, USA.
  • Hanagasi H; Neuroscience Department, Michigan State University College of Natural Science, East Lansing, MI, USA.
  • Lohmann E; Behavioural Neurology and Movement Disorders Unit, Department of Neurology, Istanbul Faculty of Medicine, Istanbul University, Istanbul, Turkey.
  • Samanci B; Department of Neurodegenerative Diseases, Hertie Institute for Clinical Brain Research, University of Tübingen, Tübingen, Germany.
  • Gurvit H; DZNE, German Center for Neurodegenerative Diseases, Tübingen, Germany.
  • Bilgic B; Behavioural Neurology and Movement Disorders Unit, Department of Neurology, Istanbul Faculty of Medicine, Istanbul University, Istanbul, Turkey.
  • Bras J; Behavioural Neurology and Movement Disorders Unit, Department of Neurology, Istanbul Faculty of Medicine, Istanbul University, Istanbul, Turkey.
  • Guerreiro R; Behavioural Neurology and Movement Disorders Unit, Department of Neurology, Istanbul Faculty of Medicine, Istanbul University, Istanbul, Turkey.
Hum Genomics ; 15(1): 48, 2021 07 28.
Article en En | MEDLINE | ID: mdl-34321086

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Predisposición Genética a la Enfermedad / Genómica / Demencia / Variaciones en el Número de Copia de ADN Tipo de estudio: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Aged / Aged80 / Female / Humans / Male / Middle aged País/Región como asunto: Asia Idioma: En Revista: Hum Genomics Asunto de la revista: GENETICA Año: 2021 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Predisposición Genética a la Enfermedad / Genómica / Demencia / Variaciones en el Número de Copia de ADN Tipo de estudio: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Aged / Aged80 / Female / Humans / Male / Middle aged País/Región como asunto: Asia Idioma: En Revista: Hum Genomics Asunto de la revista: GENETICA Año: 2021 Tipo del documento: Article País de afiliación: Estados Unidos