Influence of a nucleotide oligomerization domain 1 (NOD1) polymorphism and NOD2 mutant alleles on Crohn's disease phenotype

World Journal of Gastroenterology

Volumn 13, Issue 41, 2007, Pages 5446-5453

  Cantó, Elisabet ^a   Ricart, Elena ^b   Busquets, David ^a   Monfort, David ^a   García Planella, Esther ^a   González, Dolors ^a   Balanzó, Joaquim ^a   Rodríguez Sánchez, José L ^a   Vidal, Sílvia ^a  

^a HOSPITAL DE LA SANTA CREU I SANT PAU   (Spain)

^b HOSPITAL CLÍNIC   (Spain)

Author keywords

Crohn's disease; Nucleotide oligomerization domain 1; Nucleotide oligomerization domain 2

Indexed keywords

ARGININE; CARBOHYDRATE BINDING PROTEIN; CASPASE RECRUITMENT DOMAIN PROTEIN 15; CASPASE RECRUITMENT DOMAIN PROTEIN 4; TRYPTOPHAN; UNCLASSIFIED DRUG;

ADULT; ARTICLE; COHORT ANALYSIS; COLON OBSTRUCTION; CONTROLLED STUDY; CROHN DISEASE; DISEASE COURSE; DISEASE SEVERITY; GENE AMPLIFICATION; GENE INTERACTION; GENE MUTATION; GENE SEQUENCE; GENETIC POLYMORPHISM; GENETIC RISK; GENETIC VARIABILITY; GENOTYPE; HERITABILITY; HETEROZYGOTE; HIGH RISK POPULATION; HUMAN; MAJOR CLINICAL STUDY; MUTANT; ONSET AGE; PHENOTYPE; PREVALENCE; RESTRICTION FRAGMENT LENGTH POLYMORPHISM; SINGLE NUCLEOTIDE POLYMORPHISM; STATISTICAL SIGNIFICANCE;

EID: 35348973452     PISSN: 10079327     EISSN: None     Source Type: Journal    
DOI: 10.3748/wjg.v13.i41.5446     Document Type: Article

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