Mutation du gène NOD2 chez les patients marocains atteints de la maladie de Crohn: prévalence, étude génotypique et corrélation au phénotype de la maladie

The aim of this study was to determine the prevalence of NOD2/CARD15 gene mutations in a group of Moroccan patients with Crohn’s disease and to study its correlation with genotype-phenotypic expression. We conducted a cross-sectional case-control study over a period of 16 months. 101 patients with C...

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Detalles Bibliográficos
Autores principales: Tamzaourte, Mouna, Errabih, Ikram, Krami, Hayat, Maha, Fadlouallah, Maria, Lahmiri, Benzzoubeir, Nadia, Ouazzani, Laaziza, Sefiani, Ahmed, Ouazzani, Houria
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The African Field Epidemiology Network 2017
Materias:
Case Series
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5554695/
https://www.ncbi.nlm.nih.gov/pubmed/28819537
http://dx.doi.org/10.11604/pamj.2017.27.116.9187

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