NOD2/CARD15 variants are associated with lower weight at diagnosis in children with Crohn's disease. [electronic resource]
Producer: 20040105Description: 2479-84 p. digitalISSN:- 0002-9270
- Adolescent
- Body Weight
- Carrier Proteins -- genetics
- Case-Control Studies
- Child
- Child, Preschool
- Cohort Studies
- Crohn Disease -- diagnosis
- Female
- Genetic Predisposition to Disease
- Genetic Variation
- Genotype
- Humans
- Infant
- Intracellular Signaling Peptides and Proteins
- Male
- Mutation
- Nod2 Signaling Adaptor Protein
- Phenotype
- Polymerase Chain Reaction
- Probability
- Reference Values
- Sensitivity and Specificity
- Severity of Illness Index
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Publication Type: Comparative Study; Journal Article; Research Support, Non-U.S. Gov't
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