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...
Autores Principales: | , , , , , , , , , , , , , , , , |
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Formato: | Artículo (Article) |
Lenguaje: | Inglés (English) |
Publicado: |
2015
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Materias: | |
Acceso en línea: | http://repository.urosario.edu.co/handle/10336/19219 |