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Analysis of Cdx2 VDR gene polymorphism rs11568820 in association with multiple sclerosis in Slovaks.
Cierny, Daniel; Dobrota, Dusan; Kantorová, Ema; Malicherová, Bibiana; Skerenová, Mária; Javor, Juraj; Kurca, Egon; Lehotský, Ján.
Afiliação
  • Cierny D; Department of Clinical Biochemistry, Jessenius Faculty of Medicine, Comenius University in Bratislava and University Hospital Martin, Martin, Slovak Republic.
  • Dobrota D; Department of Clinical Biochemistry, Jessenius Faculty of Medicine, Comenius University in Bratislava and University Hospital Martin, Martin, Slovak Republic.
  • Kantorová E; Clinic of Neurology, Jessenius Faculty of Medicine, Comenius University in Bratislava and University Hospital Martin, Martin, Slovak Republic.
  • Malicherová B; Department of Clinical Biochemistry, Jessenius Faculty of Medicine, Comenius University in Bratislava and University Hospital Martin, Martin, Slovak Republic.
  • Skerenová M; Biomedical Center Martin, Jessenius Faculty of Medicine in Martin, Comenius University in Bratislava, Martin, Slovak Republic.
  • Javor J; Department of Immunology, Faculty of Medicine, Comenius University in Bratislava, Bratislava, Slovak Republic.
  • Kurca E; Clinic of Neurology, Jessenius Faculty of Medicine, Comenius University in Bratislava and University Hospital Martin, Martin, Slovak Republic.
  • Lehotský J; Department of Medical Biochemistry and BioMed, Jessenius Faculty of Medicine in Martin, Comenius University in Bratislava, Martin, Slovak Republic.
Neurol Res ; 45(10): 912-918, 2023 Oct.
Article em En | MEDLINE | ID: mdl-37581270
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Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Predisposição Genética para Doença / Esclerose Múltipla Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: Neurol Res Ano de publicação: 2023 Tipo de documento: Article
Texto completo
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XML
PubMed Links
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Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Predisposição Genética para Doença / Esclerose Múltipla Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: Neurol Res Ano de publicação: 2023 Tipo de documento: Article