Two independent genetic factors responsible for the associations of the IBD5 locus with Crohn's disease in the Czech population

Inflammatory Bowel Diseases

Volumn 17, Issue 7, 2011, Pages 1523-1529

  Hradsky, Ondrej ^a   Dusatkova, Petra ^a   Lenicek, Martin ^b   Bronsky, Jiri ^a   Duricova, Dana ^c   Nevoral, Jiri ^a   Vitek, Libor ^b   Lukas, Milan ^c   Cinek, Ondrej ^a  

^a UNIVERSITY HOSPITAL MOTOL   (Czech Republic)

^b CHARLES UNIVERSITY   (Czech Republic)

^c ISCARE IVF   (Czech Republic)

Author keywords

Crohn's disease; haplotype; IBD5; SLC22A4; SLC22A5

Indexed keywords

ADULT; ARTICLE; CAUCASIAN; CONTROLLED STUDY; CROHN DISEASE; CZECH REPUBLIC; FEMALE; GENE; GENE FREQUENCY; GENE LINKAGE DISEQUILIBRIUM; GENE LOCUS; GENETIC ASSOCIATION; GENETIC RISK; GENETIC VARIABILITY; GENOME ANALYSIS; GENOTYPE; HAPLOTYPE; HEREDITY; HUMAN; MAJOR CLINICAL STUDY; MALE; PHENOTYPE; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM; SLC22A4 GENE; SLC22A5 GENE;

ADOLESCENT; ADULT; CASE-CONTROL STUDIES; CHILD; CROHN DISEASE; CZECH REPUBLIC; FEMALE; GENE FREQUENCY; GENETIC PREDISPOSITION TO DISEASE; GENOTYPE; HAPLOTYPES; HUMANS; LINKAGE DISEQUILIBRIUM; MALE; ORGANIC CATION TRANSPORT PROTEINS; PHENOTYPE; POLYMORPHISM, SINGLE NUCLEOTIDE; YOUNG ADULT;

EID: 79958778683     PISSN: 10780998     EISSN: 15364844     Source Type: Journal    
DOI: 10.1002/ibd.21532     Document Type: Article

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