Mutation in IRF2BP2 is responsible for a Familial Form of Common Variable Immunodeficiency Disorder

BACKGROUND: Genome-wide association studies have shown a pattern of rare copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) in patients with common variable immunodeficiency disorder (CVID), which was recognizable by a Support Vector Machine (SVM) algorithm. However, rare monog...

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Publicado en:J Allergy Clin Immunol
Autores principales: Keller, Michael D, Pandey, Rahul, Li, Dong, Glessner, Joseph, Tian, Lifeng, Henrickson, Sarah E., Chinn, Ivan K., Monaco-Shawver, Linda, Heimall, Jennifer, Hou, Cuiping, Otieno, Frederick G., Jyonouchi, Soma, Calabrese, Leonard, van Montfrans, Joris, Orange, Jordan S, Hakonarson, Hakon
Formato: Artigo
Lenguaje:Inglês
Publicado: 2016
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Article
Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC4976039/
https://ncbi.nlm.nih.gov/pubmed/27016798
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.jaci.2016.01.018
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