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Volumn 127, Issue 6, 2011, Pages
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Genome-wide association identifies diverse causes of common variable immunodeficiency
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Author keywords
antibody deficiency; common variable immunodeficiency; copy number variation; genetics; genome wide association; immunodiagnostics; Primary immunodeficiency
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Indexed keywords
ADAM PROTEIN;
DISINTEGRIN;
ORIGIN RECOGNITION COMPLEX;
ORIGIN RECOGNITION COMPLEX 4L;
UNCLASSIFIED DRUG;
ARTICLE;
CHILD;
COMMON VARIABLE IMMUNODEFICIENCY;
COMORBIDITY;
CONTROLLED STUDY;
COPY NUMBER VARIATION;
EXON;
GENE;
GENE DELETION;
GENE DUPLICATION;
GENE REPLICATION;
GENETIC ANALYSIS;
GENETIC PREDISPOSITION;
GENETIC SUSCEPTIBILITY;
GENETIC VARIABILITY;
GENOTYPE;
HUMAN;
IMMUNOPATHOGENESIS;
MAJOR CLINICAL STUDY;
MAJOR HISTOCOMPATIBILITY COMPLEX;
PHENOTYPE;
PRIORITY JOURNAL;
SCHOOL CHILD;
SINGLE NUCLEOTIDE POLYMORPHISM;
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EID: 79957874121
PISSN: 00916749
EISSN: 10976825
Source Type: Journal
DOI: 10.1016/j.jaci.2011.02.039 Document Type: Article |
Times cited : (162)
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References (4)
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