Rare mutations in TNFRSF13B increase the risk of asthma symptoms in Swedish children

Genes and Immunity

Volumn 13, Issue 1, 2012, Pages 59-65

  Janzi, M ^a   Melen E ^a,b   Kull, I ^b   Wickman, M ^b,c   Hammarstrom L ^a  

^a KAROLINSKA UNIVERSITY HOSPITAL   (Sweden)

^b KAROLINSKA INSTITUTE   (Sweden)

^c STOCKHOLM SÖDER HOSPITAL   (Sweden)

Author keywords

allergy; asthma; children; genetics; IgA; TACI

Indexed keywords

IMMUNOGLOBULIN A; IMMUNOGLOBULIN E; IMMUNOGLOBULIN G; TRANSMEMBRANE ACTIVATOR AND CAML INTERACTOR;

ADULT; ARTICLE; ASTHMA; CHILD; CHILDHOOD DISEASE; CONTROLLED STUDY; GENE MUTATION; GENETIC RISK; GENETIC SUSCEPTIBILITY; HUMAN; IMMUNOGLOBULIN BLOOD LEVEL; NUCLEOTIDE SEQUENCE; PRESCHOOL CHILD; PRIORITY JOURNAL; SWEDEN; WHEEZING;

ASTHMA; CHILD; CHILD, PRESCHOOL; GENE FREQUENCY; GENETIC PREDISPOSITION TO DISEASE; GENOTYPE; HUMANS; IMMUNOGLOBULIN A; IMMUNOGLOBULIN G; MUTATION; PROGNOSIS; SWEDEN; TRANSMEMBRANE ACTIVATOR AND CAML INTERACTOR PROTEIN;

EID: 84855978239     PISSN: 14664879     EISSN: 14765470     Source Type: Journal    
DOI: 10.1038/gene.2011.55     Document Type: Article

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