Analysis of the prion protein gene in multiple system atrophy.

Chelban, Viorica; Manole, Andreea; Pihlstrøm, Lasse; Schottlaender, Lucia; Efthymiou, Stephanie; OConnor, Emer; Meissner, Wassilios G; Holton, Janice L; Houlden, Henry

Chelban, Viorica; Manole, Andreea; Pihlstrøm, Lasse; Schottlaender, Lucia; Efthymiou, Stephanie; OConnor, Emer; Meissner, Wassilios G; Holton, Janice L; Houlden, Henry.

Afiliación

Chelban V; Department of Molecular Neuroscience, UCL Institute of Neurology, London, UK; National Hospital for Neurology and Neurosurgery, Queen Square, London, UK; Department of Neurology, Medical and Pharmaceutical State University N. Testemitanu, Chisinau, Moldova. Electronic address: v.chelban@ucl.ac.uk.
Manole A; Department of Molecular Neuroscience, UCL Institute of Neurology, London, UK; National Hospital for Neurology and Neurosurgery, Queen Square, London, UK.
Pihlstrøm L; Department of Molecular Neuroscience, UCL Institute of Neurology, London, UK; National Hospital for Neurology and Neurosurgery, Queen Square, London, UK; Institute of Clinical Medicine, University of Oslo, Oslo, Norway.
Schottlaender L; Department of Molecular Neuroscience, UCL Institute of Neurology, London, UK; National Hospital for Neurology and Neurosurgery, Queen Square, London, UK.
Efthymiou S; Department of Molecular Neuroscience, UCL Institute of Neurology, London, UK; National Hospital for Neurology and Neurosurgery, Queen Square, London, UK.
OConnor E; Department of Molecular Neuroscience, UCL Institute of Neurology, London, UK; National Hospital for Neurology and Neurosurgery, Queen Square, London, UK.
Meissner WG; Univ. de Bordeaux, Institut des Maladies Neurodégénératives, UMR 5293, Bordeaux, France; CNRS, Institut des Maladies Neurodégénératives, UMR 5293, Bordeaux, France; Centre de référence atrophie multisystématisée, CHU de Bordeaux, Bordeaux, France.
Holton JL; Department of Molecular Neuroscience, UCL Institute of Neurology, London, UK; National Hospital for Neurology and Neurosurgery, Queen Square, London, UK; Reta Lila Weston Institute of Neurological Studies and Queen Square Brain Bank for Neurological Disorders, London, UK.
Houlden H; Department of Molecular Neuroscience, UCL Institute of Neurology, London, UK; National Hospital for Neurology and Neurosurgery, Queen Square, London, UK.

Neurobiol Aging ; 49: 216.e15-216.e18, 2017 01.

Article en En | MEDLINE | ID: mdl-27793473

Asunto(s)

Estudios de Asociación Genética; Atrofia de Múltiples Sistemas/genética; Proteínas Priónicas/genética; Encéfalo/diagnóstico por imagen; Codón/genética; Epistasis Genética; Exoma/genética; Femenino; Homocigoto; Humanos; Imagen por Resonancia Magnética; Masculino; Atrofia de Múltiples Sistemas/diagnóstico por imagen; Polimorfismo Genético; Factores de Riesgo; Análisis de Secuencia de ADN/métodos; alfa-Sinucleína/genética

Palabras clave

Multiple system atrophy; PRNP; Prion disease; Prion protein; Sporadic Creutzfeld-Jakob disease

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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Atrofia de Múltiples Sistemas / Estudios de Asociación Genética / Proteínas Priónicas Tipo de estudio: Etiology_studies / Prognostic_studies / Risk_factors_studies Límite: Female / Humans / Male Idioma: En Revista: Neurobiol Aging Año: 2017 Tipo del documento: Article

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