Development of a uniform, very aggressive disease phenotype in all homozygous carriers of the NOD2 mutation p.Leu1007fsX1008 with Crohn’s disease and active smoking status resulting in ileal stenosis requiring surgery

BACKGROUND: NOD2 variants are the strongest genetic predictors for susceptibility to Crohn’s disease (CD). However, the clinical value of NOD2 on an individual patient level remains controversial. We aimed to define the predictive power of the major NOD2 mutations regarding complicated CD in a large...

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Detalhes bibliográficos
Publicado no:PLoS One
Main Authors: Schnitzler, Fabian, Friedrich, Matthias, Angelberger, Marianne, Diegelmann, Julia, Stallhofer, Johannes, Wolf, Christiane, Dütschler, Joel, Truniger, Samuel, Olszak, Torsten, Beigel, Florian, Tillack, Cornelia, Lohse, Peter, Brand, Stephan
Formato: Artigo
Idioma:Inglês
Publicado em: Public Library of Science 2020
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7384669/
https://ncbi.nlm.nih.gov/pubmed/32716958
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0236421
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