Toto, A.;                     Malagrinò, F.;                     Visconti, L.;                     Troilo, F.;                     Gianni, S.    
        Unveiling the Molecular Basis of the Noonan Syndrome-Causing Mutation T42A of SHP2. Int. J. Mol. Sci. 2020, 21, 461.
    https://doi.org/10.3390/ijms21020461
    AMA Style
    
                                Toto A,                                 Malagrinò F,                                 Visconti L,                                 Troilo F,                                 Gianni S.        
                Unveiling the Molecular Basis of the Noonan Syndrome-Causing Mutation T42A of SHP2. International Journal of Molecular Sciences. 2020; 21(2):461.
        https://doi.org/10.3390/ijms21020461
    
    Chicago/Turabian Style
    
                                Toto, Angelo,                                 Francesca Malagrinò,                                 Lorenzo Visconti,                                 Francesca Troilo,                                 and Stefano Gianni.        
                2020. "Unveiling the Molecular Basis of the Noonan Syndrome-Causing Mutation T42A of SHP2" International Journal of Molecular Sciences 21, no. 2: 461.
        https://doi.org/10.3390/ijms21020461
    
    APA Style
    
                                Toto, A.,                                 Malagrinò, F.,                                 Visconti, L.,                                 Troilo, F.,                                 & Gianni, S.        
        
        (2020). Unveiling the Molecular Basis of the Noonan Syndrome-Causing Mutation T42A of SHP2. International Journal of Molecular Sciences, 21(2), 461.
        https://doi.org/10.3390/ijms21020461