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January 1, 2007World Journal of GastroenterologyOpen Access

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

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ECElisabet CantóHospital de Sant Pau

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Elisabet Cantó (2007) studied this question.

synapsesocial.com/papers/6aa8ef095b65078a7c43ebf3https://doi.org/10.3748/wjg.v13.i41.5446
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Also Consider

Synapse has enriched 3 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1CARD15/NOD2 gene variants are associated with familially occurring and complicated forms of Crohn’s disease2003 · 271 citations
  2. 2Early-onset sarcoidosis and CARD15 mutations with constitutive nuclear factor- B activation: common genetic etiology with Blau syndrome2004 · 484 citations
  3. 3Behaviour of Crohn's disease according to the Vienna classification: changing pattern over the course of the disease2001 · 1,012 citations