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...

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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: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4450850/
https://www.ncbi.nlm.nih.gov/pubmed/26031516
http://dx.doi.org/10.1186/s12967-015-0525-x

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4450850/
https://www.ncbi.nlm.nih.gov/pubmed/26031516
http://dx.doi.org/10.1186/s12967-015-0525-x

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