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
The Journal of allergy and clinical immunology
CD11b Antigen; Chromosomes, Human, Pair 16; Common Variable Immunodeficiency; Genetic Predisposition to Disease; Polymorphism, Single Nucleotide; RNA-Binding Protein FUS
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
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.
Rare variants at 16p11.2 are associated with common variable immunodeficiency.