Application of whole genome and RNA sequencing to investigate the genomic landscape of common variable immunodeficiency disorders

Common Variable Immunodeficiency Disorders (CVIDs) are the most prevalent cause of primary antibody failure. CVIDs are highly variable and a genetic causes have been identified in <5% of patients. Here, we performed whole genome sequencing (WGS) of 34 CVID patients (94% sporadic) and combined the...

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Detalles Bibliográficos
Autores principales: van Schouwenburg, Pauline A., Davenport, Emma E., Kienzler, Anne-Kathrin, Marwah, Ishita, Wright, Benjamin, Lucas, Mary, Malinauskas, Tomas, Martin, Hilary C., Lockstone, Helen E., Cazier, Jean-Baptiste, Chapel, Helen M., Knight, Julian C., Patel, Smita Y.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2015
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4601528/
https://www.ncbi.nlm.nih.gov/pubmed/26122175
http://dx.doi.org/10.1016/j.clim.2015.05.020

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4601528/
https://www.ncbi.nlm.nih.gov/pubmed/26122175
http://dx.doi.org/10.1016/j.clim.2015.05.020

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