Associated Papers
Inborn Errors in the LRR Domain of Nod2 and Their Potential Consequences on the Function of the Receptor.
Alipoor SD et al.
Cells, 2021
A Novel Rare Missense Variation of the NOD2 Gene: Evidencesof Implication in Crohn's Disease.
Frade-Proud'Hon-Clerc S et al.
International Journal of Molecular Sciences, 2019
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