3020insC mutation within the NOD2 gene in Crohn's disease: Frequency and association with clinical pattern in an Italian population [3]

Digestive and Liver Disease

Volumn 34, Issue 2, 2002, Pages 153-

  Vavassori, P ^a   Borgiani, P ^a   D'Apice, M R ^a   De Nigris, F ^a   Del Vecchio Blanco, G ^a   Monteleone, I ^a   Biancone, L ^a   Novelli, G ^a   Pallone, F ^a  

^a UNIVERSITY OF ROME TOR VERGATA   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

CASPASE RECRUITMENT DOMAIN PROTEIN 15; CYTOSINE; DNA; GENE PRODUCT; UNCLASSIFIED DRUG;

ADULT; AGED; APPENDECTOMY; BLOOD SAMPLING; CLINICAL FEATURE; CONTROLLED STUDY; CROHN DISEASE; DISEASE DURATION; DNA DETERMINATION; FAMILY HISTORY; FEMALE; GENE FREQUENCY; GENE INSERTION; GENE MUTATION; GENETIC ASSOCIATION; GENOTYPE; HETEROZYGOSITY; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; HOMOZYGOSITY; HUMAN; INTESTINE RESECTION; ITALY; LETTER; MAJOR CLINICAL STUDY; MALE; POLYMERASE CHAIN REACTION; POPULATION RESEARCH; POSTOPERATIVE COMPLICATION; REGRESSION ANALYSIS; RISK ASSESSMENT; RISK FACTOR; SINGLE NUCLEOTIDE POLYMORPHISM; STATISTICAL ANALYSIS;

EID: 0012135426     PISSN: 15908658     EISSN: None     Source Type: Journal    
DOI: 10.1016/S1590-8658(02)80249-3     Document Type: Letter

References (3)

1. Association of NOD2 leucine-rich repeat variants with the susceptibility to Crohn's disease
2. A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease
3. Association between insertion mutation in NOD2 gene and Crohn's disease in German and British populations