Title : Acute intestinal obstruction and NOD2/CARD15 mutations among Italian Crohn's disease patients.

Pub. Date : 2004 Sep-Oct

PMID : 15638227






4 Functional Relationships(s)
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1 UNLABELLED: Three CARD15 mutations (SNP8, SNP12, SNP13) were significantly associated with CD, however ethnic variations and genotype-phenotype relationships are still to be defined. Cadmium nucleotide binding oligomerization domain containing 2 Homo sapiens
2 AIMS: To evaluate the prevalence of three CARD15 mutations in 91 in-out consecutive CD, 109 Ulcerative Colitis (UC), 101 healthy controls; to examine the genotype-phenotype relationships among italian pts with CD. Cadmium nucleotide binding oligomerization domain containing 2 Homo sapiens
3 RESULTS: The allelic and genotype frequencies of CARD15 mutations were significantly associated to CD. Cadmium nucleotide binding oligomerization domain containing 2 Homo sapiens
4 CONCLUSIONS: Our data confirms that CARD15 mutations are significantly associated with CD also in Italian population and with small bowel location (OM and CET genotype). Cadmium nucleotide binding oligomerization domain containing 2 Homo sapiens