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Assessment of common variability and expression quantitative trait loci for genome-wide associations for progressive supranuclear palsy.
Ferrari, Raffaele; Ryten, Mina; Simone, Roberto; Trabzuni, Daniah; Nicolaou, Nayia; Nicolaou, Naiya; Hondhamuni, Geshanthi; Ramasamy, Adaikalavan; Vandrovcova, Jana; Weale, Michael E; Lees, Andrew J; Momeni, Parastoo; Hardy, John; de Silva, Rohan.
Afiliación
  • Ferrari R; Laboratory of Neurogenetics, Department of Internal Medicine, Texas Tech University Health Sciences Center, Lubbock, TX, USA; Reta Lila Weston Institute, UCL Institute of Neurology, London, UK; Department of Molecular Neuroscience, UCL Institute of Neurology, London, UK.
  • Ryten M; Department of Molecular Neuroscience, UCL Institute of Neurology, London, UK.
  • Simone R; Reta Lila Weston Institute, UCL Institute of Neurology, London, UK; Department of Molecular Neuroscience, UCL Institute of Neurology, London, UK.
  • Trabzuni D; Department of Molecular Neuroscience, UCL Institute of Neurology, London, UK; Department of Genetics, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia.
  • Nicolaou N; Reta Lila Weston Institute, UCL Institute of Neurology, London, UK; Department of Molecular Neuroscience, UCL Institute of Neurology, London, UK.
  • Nicolaou N; Reta Lila Weston Institute, UCL Institute of Neurology, London, UK; Department of Molecular Neuroscience, UCL Institute of Neurology, London, UK.
  • Hondhamuni G; Reta Lila Weston Institute, UCL Institute of Neurology, London, UK; Department of Molecular Neuroscience, UCL Institute of Neurology, London, UK.
  • Ramasamy A; Department of Molecular Neuroscience, UCL Institute of Neurology, London, UK; Department of Medical and Molecular Genetics, King's College London, Guy's Hospital, London, UK.
  • Vandrovcova J; Reta Lila Weston Institute, UCL Institute of Neurology, London, UK; Department of Molecular Neuroscience, UCL Institute of Neurology, London, UK.
  • Weale ME; Department of Medical and Molecular Genetics, King's College London, Guy's Hospital, London, UK.
  • Lees AJ; Reta Lila Weston Institute, UCL Institute of Neurology, London, UK.
  • Momeni P; Laboratory of Neurogenetics, Department of Internal Medicine, Texas Tech University Health Sciences Center, Lubbock, TX, USA.
  • Hardy J; Reta Lila Weston Institute, UCL Institute of Neurology, London, UK; Department of Molecular Neuroscience, UCL Institute of Neurology, London, UK.
  • de Silva R; Reta Lila Weston Institute, UCL Institute of Neurology, London, UK; Department of Molecular Neuroscience, UCL Institute of Neurology, London, UK. Electronic address: r.desilva@ucl.ac.uk.
Neurobiol Aging ; 35(6): 1514.e1-12, 2014 Jun.
Article en En | MEDLINE | ID: mdl-24503276

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Variación Genética / Parálisis Supranuclear Progresiva / Expresión Génica / Sitios de Carácter Cuantitativo / Estudio de Asociación del Genoma Completo Tipo de estudio: Etiology_studies / Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Neurobiol Aging Año: 2014 Tipo del documento: Article País de afiliación: Reino Unido

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Variación Genética / Parálisis Supranuclear Progresiva / Expresión Génica / Sitios de Carácter Cuantitativo / Estudio de Asociación del Genoma Completo Tipo de estudio: Etiology_studies / Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Neurobiol Aging Año: 2014 Tipo del documento: Article País de afiliación: Reino Unido