Novel and rare functional genomic variants in multiple autoimmune syndrome and Sjögren's syndrome

Background: Multiple autoimmune syndrome (MAS), an extreme phenotype of autoimmune disorders, is a very well suited trait to tackle genomic variants of these conditions. Whole exome sequencing (WES) is a widely used strategy for detection of protein coding and splicing variants associated with inher...

Descripción completa

Detalles Bibliográficos
Autores Principales: Johar, Angad S, Mastronardi, Claudio, Rojas-Villarraga, Adriana, Patel, Hardip R, Chuah, Aaron, Peng, Kaiman, Higgins, Angela, Milburn, Peter, Palmer, Stephanie, Silva‑Lara, Maria Fernanda, Velez, Jorge I, Andrews, Dan, Field, Matthew, Huttley, Gavin, Goodnow, Chris, Anaya, Juan-Manuel, Arcos-Burgos, Mauricio
Formato: Artículo (Article)
Lenguaje:Inglés (English)
Publicado: 2015
Materias:
Acceso en línea:http://repository.urosario.edu.co/handle/10336/19219