Behçet’s disease and genetic interactions between HLA-B*51 and variants in genes of autoinflammatory syndromes

Behçet’s disease (BD) is an immune-mediated systemic disorder with a well-established genetic base. In a previous study, using a next generation sequencing approach, we found many rare variants and some functional polymorphisms in genes related to autoinflammatory syndromes (AID): CECR1, MEFV, MVK,...

Descripción completa

Detalles Bibliográficos
Autores principales: Burillo-Sanz, Sergio, Montes-Cano, Marco-Antonio, García-Lozano, José-Raúl, Olivas-Martínez, Israel, Ortego-Centeno, Norberto, García-Hernández, Francisco-José, Espinosa, Gerard, Graña-Gil, Genaro, Sánchez-Bursón, Juan, Juliá, María Rosa, Solans, Roser, Blanco, Ricardo, Barnosi-Marín, Ana-Celia, Gómez de la Torre, Ricardo, Fanlo, Patricia, Rodríguez-Carballeira, Mónica, Rodríguez-Rodríguez, Luis, Camps, Teresa, Castañeda, Santos, Alegre-Sancho, Juan-Jose, Martín, Javier, González-Escribano, María Francisca
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6391494/
https://www.ncbi.nlm.nih.gov/pubmed/30808881
http://dx.doi.org/10.1038/s41598-019-39113-5

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6391494/
https://www.ncbi.nlm.nih.gov/pubmed/30808881
http://dx.doi.org/10.1038/s41598-019-39113-5

Ejemplares similares