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Frade-Proud’Hon-Clerc S, Smol T, Frenois F, Sand O, Vaillant E, Dhennin V, Bonnefond A, Froguel P, Fumery M, Guillon-Dellac N, et al. A Novel Rare Missense Variation of the NOD2 Gene: Evidences of Implication in Crohn’s Disease. International Journal of Molecular Sciences. 2019; 20(4):835. https://doi.org/10.3390/ijms20040835

Frade-Proud’Hon-Clerc, Sara, Thomas Smol, Frédéric Frenois, Olivier Sand, Emmanuel Vaillant, Véronique Dhennin, Amélie Bonnefond, Philippe Froguel, Mathurin Fumery, Nathalie Guillon-Dellac, and et al. 2019. "A Novel Rare Missense Variation of the NOD2 Gene: Evidences of Implication in Crohn’s Disease" International Journal of Molecular Sciences 20, no. 4: 835. https://doi.org/10.3390/ijms20040835

Frade-Proud’Hon-Clerc, S., Smol, T., Frenois, F., Sand, O., Vaillant, E., Dhennin, V., Bonnefond, A., Froguel, P., Fumery, M., Guillon-Dellac, N., Gower-Rousseau, C., & Vasseur, F. (2019). A Novel Rare Missense Variation of the NOD2 Gene: Evidences of Implication in Crohn’s Disease. International Journal of Molecular Sciences, 20(4), 835. https://doi.org/10.3390/ijms20040835