Autophagy genes variants and paediatric Crohn's disease phenotype: a single-centre experience. [electronic resource]
- Digestive and liver disease : official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver Jun 2014
- 512-7 p. digital
Publication Type: Journal Article
1878-3562
10.1016/j.dld.2014.02.016 doi
Adolescent Autophagy--genetics Autophagy-Related Proteins C-Reactive Protein--metabolism Carrier Proteins--genetics Child Child, Preschool Constriction, Pathologic--genetics Crohn Disease--drug therapy Feces--chemistry Female GTP-Binding Proteins--genetics Heterozygote Homozygote Humans Ileitis--genetics Immunosuppressive Agents--therapeutic use Infant Leukocyte L1 Antigen Complex--analysis Male Nod2 Signaling Adaptor Protein--genetics Phenotype Polymorphism, Single Nucleotide Recurrence Severity of Illness Index