CARD15/NOD2 risk alleles in the development of Crohn's disease in the Australian population

Annals of Human Genetics

Volumn 67, Issue 1, 2003, Pages 35-41

  Cavanaugh, Juleen A ^a   Adams, K E ^a   Quak, E J ^a   Bryce, M E ^a   O'Callaghan, N J ^b   Rodgers, H J ^a   Magarry, G R ^a   Butler, W J ^c   Eaden, J A ^c   Roberts Thomson, I C ^c   Pavli, P ^a   Wilson, S R ^d   Callen, D F ^b  

^a CANBERRA HOSPITAL   (Australia)

^b WOMEN S AND CHILDREN S HOSPITAL   (Australia)

^c QUEEN ELIZABETH HOSPITAL   (Australia)

^d AUSTRALIAN NATIONAL UNIVERSITY   (Australia)

Author keywords

[No Author keywords available]

Indexed keywords

ARGININE; CASPASE RECRUITMENT DOMAIN PROTEIN 15; CYTOSINE; GLYCINE; GUANINE; THYMINE; TRYPTOPHAN; CARD15 PROTEIN, HUMAN; CARRIER PROTEIN; SIGNAL PEPTIDE;

ALLELE; ARTICLE; AUSTRALIA; CHROMOSOME 16; CONTROLLED STUDY; CROHN DISEASE; ENTERITIS; FAMILY; FEMALE; FRAMESHIFT MUTATION; GENE FREQUENCY; GENE LOCUS; GENETIC ASSOCIATION; GENETIC RISK; GENETIC SUSCEPTIBILITY; HETEROZYGOSITY; HOMOZYGOSITY; HUMAN; MAJOR CLINICAL STUDY; MALE; NUCLEOTIDE SEQUENCE; POLYMERASE CHAIN REACTION; POPULATION GENETICS; PRIORITY JOURNAL; RESTRICTION FRAGMENT LENGTH POLYMORPHISM; STATISTICAL SIGNIFICANCE; ETHNOLOGY; GENETIC LINKAGE; GENETIC PREDISPOSITION; GENETICS; GENOTYPE; MUTATION; RISK FACTOR;

ALLELES; AUSTRALIA; CARRIER PROTEINS; CHROMOSOMES, HUMAN, PAIR 16; CROHN DISEASE; GENE FREQUENCY; GENETIC PREDISPOSITION TO DISEASE; GENOTYPE; HUMANS; INTRACELLULAR SIGNALING PEPTIDES AND PROTEINS; LINKAGE (GENETICS); MUTATION; NOD2 SIGNALING ADAPTOR PROTEIN; RISK FACTORS;

EID: 0038136125     PISSN: 00034800     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1469-1809.2003.00006.x     Document Type: Article

References (20)

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