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. Int. J. Mol. Sci. 2019, 20, 835.
    https://doi.org/10.3390/ijms20040835
    AMA Style
    
                                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
    
    Chicago/Turabian Style
    
                                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
    
    APA Style
    
                                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