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Lack of Association Between the CCR5-delta32 Polymorphism and Neurodegenerative Disorders.
Wojta, Kevin J; Ayer, Ariane H; Ramos, Eliana M; Nguyen, Peter D; Karydas, Anna M; Yokoyama, Jennifer S; Kramer, Joel; Lee, Suzee E; Boxer, Adam; Miller, Bruce L; Coppola, Giovanni.
Afiliação
  • Wojta KJ; Department of Psychiatry, Semel Institute for Neuroscience and Human Behavior, David Geffen School of Medicine, University of California Los Angeles, Los Angeles.
  • Ayer AH; Department of Psychiatry, Semel Institute for Neuroscience and Human Behavior, David Geffen School of Medicine, University of California Los Angeles, Los Angeles.
  • Ramos EM; Department of Psychiatry, Semel Institute for Neuroscience and Human Behavior, David Geffen School of Medicine, University of California Los Angeles, Los Angeles.
  • Nguyen PD; Department of Psychiatry, Semel Institute for Neuroscience and Human Behavior, David Geffen School of Medicine, University of California Los Angeles, Los Angeles.
  • Karydas AM; Department of Neurology, Memory and Aging Center, University of California San Francisco, San Francisco, CA.
  • Yokoyama JS; Department of Neurology, Memory and Aging Center, University of California San Francisco, San Francisco, CA.
  • Kramer J; Department of Neurology, Memory and Aging Center, University of California San Francisco, San Francisco, CA.
  • Lee SE; Department of Neurology, Memory and Aging Center, University of California San Francisco, San Francisco, CA.
  • Boxer A; Department of Neurology, Memory and Aging Center, University of California San Francisco, San Francisco, CA.
  • Miller BL; Department of Neurology, Memory and Aging Center, University of California San Francisco, San Francisco, CA.
  • Coppola G; Department of Psychiatry, Semel Institute for Neuroscience and Human Behavior, David Geffen School of Medicine, University of California Los Angeles, Los Angeles.
Alzheimer Dis Assoc Disord ; 34(3): 244-247, 2020.
Article em En | MEDLINE | ID: mdl-31972607
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Polimorfismo Genético / Idade de Início / Doenças Neurodegenerativas / Receptores CCR5 Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Humans / Middle aged País como assunto: America do norte Idioma: En Ano de publicação: 2020 Tipo de documento: Article
Texto completo
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PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Polimorfismo Genético / Idade de Início / Doenças Neurodegenerativas / Receptores CCR5 Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Humans / Middle aged País como assunto: America do norte Idioma: En Ano de publicação: 2020 Tipo de documento: Article