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Identification of LRRK2 missense variants in the accelerating medicines partnership Parkinson's disease cohort.
Bryant, Nicole; Malpeli, Nicole; Ziaee, Julia; Blauwendraat, Cornelis; Liu, Zhiyong; West, Andrew B.
Afiliação
  • Bryant N; Duke Center for Neurodegeneration and Neurotherapeutics Research, Departments of Pharmacology and Cancer Biology, and Neurology, Duke University, Durham, NC 27710 USA.
  • Malpeli N; Duke Center for Neurodegeneration and Neurotherapeutics Research, Departments of Pharmacology and Cancer Biology, and Neurology, Duke University, Durham, NC 27710 USA.
  • Ziaee J; Duke Center for Neurodegeneration and Neurotherapeutics Research, Departments of Pharmacology and Cancer Biology, and Neurology, Duke University, Durham, NC 27710 USA.
  • Blauwendraat C; Laboratory of Neurogenetics, National Institute on Aging, National Institutes of Health, Bethesda, MD 20892, USA.
  • Liu Z; Duke Center for Neurodegeneration and Neurotherapeutics Research, Departments of Pharmacology and Cancer Biology, and Neurology, Duke University, Durham, NC 27710 USA.
  • West AB; Duke Center for Neurodegeneration and Neurotherapeutics Research, Departments of Pharmacology and Cancer Biology, and Neurology, Duke University, Durham, NC 27710 USA.
Hum Mol Genet ; 30(6): 454-466, 2021 04 30.
Article em En | MEDLINE | ID: mdl-33640967
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doença de Parkinson / Predisposição Genética para Doença / Mutação de Sentido Incorreto / Estudo de Associação Genômica Ampla / Serina-Treonina Proteína Quinase-2 com Repetições Ricas em Leucina Tipo de estudo: Diagnostic_studies / Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2021 Tipo de documento: Article
Texto completo
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doença de Parkinson / Predisposição Genética para Doença / Mutação de Sentido Incorreto / Estudo de Associação Genômica Ampla / Serina-Treonina Proteína Quinase-2 com Repetições Ricas em Leucina Tipo de estudo: Diagnostic_studies / Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2021 Tipo de documento: Article