Rare variants at 16p11.2 are associated with common variable immunodeficiency.
PubMed Identifier: 25678086
author list: Maggadottir SM, Li J, Glessner JT, Li YR, Wei Z, Chang X, Mentch FD, Thomas KA, Kim CE, Zhao Y, Hou C, Wang F, J?rgensen SF, Perez EE, Sullivan KE, Orange JS, Karlsen TH, Chapel H, Cunningham-Rundles C, Hakonarson H
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published in: The Journal of allergy and clinical immunology
has major subject area list: CD11b Antigen; Chromosomes, Human, Pair 16; Common Variable Immunodeficiency; Genetic Predisposition to Disease; Polymorphism, Single Nucleotide; RNA-Binding Protein FUS
has minor subject area list: Adult; B-Lymphocytes; Case-Control Studies; Child, Preschool; Cohort Studies; Enhancer Elements, Genetic; Female; Genetic Loci; Humans; Immunologic Memory; Linkage Disequilibrium; Male; Promoter Regions, Genetic
information resource reference: Maggadottir SM, Li J, Glessner JT, Li YR, Wei Z, Chang X, Mentch FD, Thomas KA, Kim CE, Zhao Y, Hou C, Wang F, J?rgensen SF, Perez EE, Sullivan KE, Orange JS, Karlsen TH, Chapel H, Cunningham-Rundles C, Hakonarson H. Rare variants at 16p11.2 are associated with common variable immunodeficiency. J Allergy Clin Immunol. 2015 Jun; 135(6):1569-77.
journal title abbreviation: J Allergy Clin Immunol
publication date: 2015-02-10T00:00:00
year: 2015
type: Academic Article
type: Article
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has subject area: Chromosomes, Human, Pair 16
has subject area: Common Variable Immunodeficiency
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has subject area: Genetic Loci
has subject area: Humans
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linked information resource: Rare variants at 16p11.2 are associated with common variable immunodeficiency.

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