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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
6
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pubmed:dateCreated |
2007-5-9
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pubmed:abstractText |
The single nucleotide variations R702W, G908R and L1007fs in the CARD15 gene have been found to be independently associated with Crohn's disease. The aim of this study was to evaluate the prevalence of these gene variations in Dutch multiple inflammatory bowel disease-affected families, in sporadic inflammatory bowel disease patients and in healthy controls.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
|
|
pubmed:status |
MEDLINE
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pubmed:month |
Jun
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pubmed:issn |
0954-691X
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pubmed:author |
|
|
pubmed:issnType |
Print
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pubmed:volume |
19
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
449-59
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pubmed:dateRevised |
2009-10-16
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pubmed:meshHeading |
pubmed-meshheading:17489054-Adult,
pubmed-meshheading:17489054-Aged,
pubmed-meshheading:17489054-Colitis, Ulcerative,
pubmed-meshheading:17489054-Crohn Disease,
pubmed-meshheading:17489054-Family Health,
pubmed-meshheading:17489054-Female,
pubmed-meshheading:17489054-Gene Frequency,
pubmed-meshheading:17489054-Genotype,
pubmed-meshheading:17489054-Humans,
pubmed-meshheading:17489054-Inflammatory Bowel Diseases,
pubmed-meshheading:17489054-Male,
pubmed-meshheading:17489054-Middle Aged,
pubmed-meshheading:17489054-Mutation,
pubmed-meshheading:17489054-Netherlands,
pubmed-meshheading:17489054-Nod2 Signaling Adaptor Protein,
pubmed-meshheading:17489054-Pedigree,
pubmed-meshheading:17489054-Phenotype,
pubmed-meshheading:17489054-Prevalence
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pubmed:year |
2007
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pubmed:articleTitle |
CARD15 mutations in Dutch familial and sporadic inflammatory bowel disease and an overview of European studies.
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pubmed:affiliation |
Department of Gastroenterology and Hepatology, Erasmus MC University Medical Center, Rotterdam, The Netherlands. k.v.d.linde@znb.nl
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pubmed:publicationType |
Journal Article,
Review,
Research Support, Non-U.S. Gov't
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