Genetic variants of 17q21 are associated with childhood-onset asthma and related phenotypes in a northeastern Han Chinese population: A case-control study

Tissue Antigens

Volumn 83, Issue 5, 2014, Pages 330-336

  Yu, X ^a,b   Yu, C ^a   Ren, Z ^a   Deng, Y ^a   Song, J ^a   Zhang, H ^a   Zhou, H ^a  

^a HARBIN MEDICAL UNIVERSITY   (China)

^b Harbin Children's Hospital 150020   (China)

Author keywords

Childhood onset asthma; Common variants; Han Chinese population; ORMDL3 locus; Single nucleotide polymorphism

Indexed keywords

IMMUNOGLOBULIN E; MEMBRANE PROTEIN; ORMDL3 PROTEIN, HUMAN;

ALLELE; ASIAN CONTINENTAL ANCESTRY GROUP; ASTHMA; BIOLOGICAL MODEL; CASE CONTROL STUDY; CHILD; CHROMOSOME 17; ETHNOLOGY; FEMALE; GENE FREQUENCY; GENE LOCUS; GENETIC ASSOCIATION; GENETIC PREDISPOSITION; GENETICS; HUMAN; IMMUNOLOGY; MALE; ONSET AGE; PHENOTYPE; PRESCHOOL CHILD; RISK FACTOR; SINGLE NUCLEOTIDE POLYMORPHISM;

AGE OF ONSET; ALLELES; ASIAN CONTINENTAL ANCESTRY GROUP; ASTHMA; CASE-CONTROL STUDIES; CHILD; CHILD, PRESCHOOL; CHROMOSOMES, HUMAN, PAIR 17; FEMALE; GENE FREQUENCY; GENETIC LOCI; GENETIC PREDISPOSITION TO DISEASE; GENOME-WIDE ASSOCIATION STUDY; HUMANS; IMMUNOGLOBULIN E; MALE; MEMBRANE PROTEINS; MODELS, GENETIC; PHENOTYPE; POLYMORPHISM, SINGLE NUCLEOTIDE; RISK FACTORS;

EID: 84898800582     PISSN: 00012815     EISSN: 13990039     Source Type: Journal    
DOI: 10.1111/tan.12342     Document Type: Article

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