CARD15/NOD2 mutational analysis and genotype-phenotype correlation in 612 patients with inflammatory bowel disease.
By S. Lesage, H. Zouali, J. Cézard, J. Colombel, J. Belaiche, S. Almér, C. Tysk, C. O'Morain, M. Gassull, V. Binder and 9 more. American Journal of Human Genetics, 2002
1,033 citations recorded by the source corpus.
Subfields: Genetics, Infectious Diseases, Surgery
View Paper: https://www.semanticscholar.org/paper/d073610fe1c0bc281d50fda8165de06de683fb26
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Citations in the corpus
- Horror autoinflammaticus: the molecular pathophysiology of autoinflammatory disease (*). (2009, background): “While CD mutations are found throughout NOD2, three mutations in the Cterminal third account for 80% of NOD2 CD variants (169).”
- A Proposed Classification of the Immunological Diseases (2006, background): “mutation is associated with site-specific involvement of the ileum and severe stricturing disease [”