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

Pons, Roser; Kekou, Kyriaki; Antonellou, Roubina; Svingou, Maria; Kanavakis, Emmanouel; Stefanis, Leonidas.

Afiliação

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 em En | MEDLINE | ID: mdl-27666733

Assuntos

Doença de Parkinson/genética; Doença de Parkinson/fisiopatologia; Tirosina 3-Mono-Oxigenase/genética; Adulto; Idade de Início; Estudos de Coortes; Feminino; Grécia/epidemiologia; Humanos; Masculino; Pessoa de Meia-Idade; Mutação; Doença de Parkinson/epidemiologia

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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doença de Parkinson / Tirosina 3-Mono-Oxigenase Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Risk_factors_studies Limite: Adult / Female / Humans / Male / Middle aged País como assunto: Europa Idioma: En Ano de publicação: 2016 Tipo de documento: Article

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