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Analysis of a founder mutation in the TH gene in a cohort of greek patients with Parkinson's disease.
Pons, Roser; Kekou, Kyriaki; Antonellou, Roubina; Svingou, Maria; Kanavakis, Emmanouel; Stefanis, Leonidas.
Afiliación
  • Pons R; First Department of Pediatrics, Agia Sophia Children's Hospital, National and Kapodistrian University of Athens, Greece.
  • Kekou K; Department of Medical Genetics, Agia Sophia Children's Hospital, National and Kapodistrian University of Athens, Greece.
  • Antonellou R; Second Department of Neurology, Attikon University Hospital, National and Kapodistrian University of Athens, Athens, Greece.
  • Svingou M; Department of Medical Genetics, Agia Sophia Children's Hospital, National and Kapodistrian University of Athens, Greece.
  • Kanavakis E; Department of Medical Genetics, Agia Sophia Children's Hospital, National and Kapodistrian University of Athens, Greece.
  • Stefanis L; Second Department of Neurology, Attikon University Hospital, National and Kapodistrian University of Athens, Athens, Greece.
Mov Disord ; 31(11): 1753-1754, 2016 11.
Article en En | MEDLINE | ID: mdl-27666733

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Enfermedad de Parkinson / Tirosina 3-Monooxigenasa Tipo de estudio: Etiology_studies / Incidence_studies / Observational_studies / Risk_factors_studies Límite: Adult / Female / Humans / Male / Middle aged País/Región como asunto: Europa Idioma: En Revista: Mov Disord Asunto de la revista: NEUROLOGIA Año: 2016 Tipo del documento: Article País de afiliación: Grecia

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Enfermedad de Parkinson / Tirosina 3-Monooxigenasa Tipo de estudio: Etiology_studies / Incidence_studies / Observational_studies / Risk_factors_studies Límite: Adult / Female / Humans / Male / Middle aged País/Región como asunto: Europa Idioma: En Revista: Mov Disord Asunto de la revista: NEUROLOGIA Año: 2016 Tipo del documento: Article País de afiliación: Grecia