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