Association between Interleukin-10 Gene Polymorphisms and Behcet's Disease Susceptibility: Evidence from a Meta-Analysis.

Li, Xue-Feng; Huang, Zhi-Zhen; Hu, Yuan-Yuan; Niu, Yu-Ming; Cai, Jun-Wei

Li, Xue-Feng; Huang, Zhi-Zhen; Hu, Yuan-Yuan; Niu, Yu-Ming; Cai, Jun-Wei.

Afiliação

Li XF; Department of Endocrinology, Hubei Key Laboratory of Embryonic Stem Cell Research, Taihe Hospital, Hubei University of Medicine, Shiyan 442000, China.
Huang ZZ; Department of Stomatology, Evidence-Based Medicine and Clinical Research, Hubei Key Laboratory of Embryonic Stem Cell Research, Taihe Hospital, Hubei University of Medicine, Shiyan 442000, China.
Hu YY; Department of Stomatology, Evidence-Based Medicine and Clinical Research, Hubei Key Laboratory of Embryonic Stem Cell Research, Taihe Hospital, Hubei University of Medicine, Shiyan 442000, China.
Niu YM; Department of Endocrinology, Hubei Key Laboratory of Embryonic Stem Cell Research, Taihe Hospital, Hubei University of Medicine, Shiyan 442000, China.
Cai JW; Department of Stomatology, Evidence-Based Medicine and Clinical Research, Hubei Key Laboratory of Embryonic Stem Cell Research, Taihe Hospital, Hubei University of Medicine, Shiyan 442000, China.

J Immunol Res ; 2020: 9382609, 2020.

Article em En | MEDLINE | ID: mdl-32656270

Assuntos

Síndrome de Behçet/genética; Genótipo; Interleucina-10/genética; Polimorfismo de Nucleotídeo Único/genética; Frequência do Gene; Estudos de Associação Genética; Predisposição Genética para Doença; Haplótipos; Humanos; Risco

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome de Behçet / Interleucina-10 / Polimorfismo de Nucleotídeo Único / Genótipo Tipo de estudo: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies / Systematic_reviews Limite: Humans Idioma: En Ano de publicação: 2020 Tipo de documento: Article

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