Relationship between the 17q21 locus and adult asthma in a Czech population

Human Immunology

Volumn 72, Issue 10, 2011, Pages 921-925

  Hrdlickova, Barbara ^a,b   Holla, Lydie Izakovicova ^a  

^a MASARYK UNIVERSITY   (Czech Republic)

^b UNIVERSITY HOSPITAL BRNO   (Czech Republic)

Author keywords

Allergic asthma; Caucasian; ORMDL3; Single nucleotide polymorphism

Indexed keywords

IMMUNOGLOBULIN E;

ADULT; ARTICLE; ASTHMA; CHROMOSOME 17Q; CONTROLLED STUDY; CZECH REPUBLIC; FEMALE; GENE LINKAGE DISEQUILIBRIUM; GENE LOCUS; GENETIC ASSOCIATION; GENETIC RISK; GENETIC VARIABILITY; GENOTYPE; HAPLOTYPE; HUMAN; LUNG FUNCTION; MAJOR CLINICAL STUDY; MALE; ORMDL3 GENE; PRIORITY JOURNAL; SEX DIFFERENCE; SINGLE NUCLEOTIDE POLYMORPHISM;

ADOLESCENT; ADULT; ASTHMA; CASE-CONTROL STUDIES; CHROMOSOMES, HUMAN, PAIR 17; CZECH REPUBLIC; EUROPEAN CONTINENTAL ANCESTRY GROUP; FEMALE; GENE FREQUENCY; GENETIC LOCI; GENETIC PREDISPOSITION TO DISEASE; GENOTYPE; HAPLOTYPES; HUMANS; HYPERSENSITIVITY, IMMEDIATE; IMMUNOGLOBULIN E; LINKAGE DISEQUILIBRIUM; MALE; MEMBRANE PROTEINS; MIDDLE AGED; ODDS RATIO; POLYMORPHISM, SINGLE NUCLEOTIDE; RISK FACTORS;

EID: 80052961827     PISSN: 01988859     EISSN: 18791166     Source Type: Journal    
DOI: 10.1016/j.humimm.2011.07.309     Document Type: Article

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