TIM-3 genetic variants and risk of Behçet disease in the Iranian population
An. bras. dermatol; 94 (4), 2019
Abstract: Background: Behçet disease is a prototypical systemic autoimmune disease, caused by a complex interplay between environmental and genetic factors. The transmembrane immunoglobulin and mucin domain-3 (TIM-3) is a distinct member of the TIM family that is preferentially expressed on Th1 cells a...
Alelos, Síndrome de Behçet/genética, Estudios de Casos y Controles, Frecuencia de los Genes, Estudios de Asociación Genética, Receptor 2 Celular del Virus de la Hepatitis A/genética, Irán, Modelos Logísticos, Reacción en Cadena de la Polimerasa Multiplex, Polimorfismo de Nucleótido Simple, Medición de Riesgo, Factores de Riesgo