Visibelli, A.; Finetti, R.; Niccolai, P.; Trezza, A.; Spiga, O.; Santucci, A.; Niccolai, N.
Profiling of Protein-Coding Missense Mutations in Mendelian Rare Diseases: Clues from Structural Bioinformatics. Int. J. Mol. Sci. 2025, 26, 4072.
https://doi.org/10.3390/ijms26094072
AMA Style
Visibelli A, Finetti R, Niccolai P, Trezza A, Spiga O, Santucci A, Niccolai N.
Profiling of Protein-Coding Missense Mutations in Mendelian Rare Diseases: Clues from Structural Bioinformatics. International Journal of Molecular Sciences. 2025; 26(9):4072.
https://doi.org/10.3390/ijms26094072
Chicago/Turabian Style
Visibelli, Anna, Rebecca Finetti, Piero Niccolai, Alfonso Trezza, Ottavia Spiga, Annalisa Santucci, and Neri Niccolai.
2025. "Profiling of Protein-Coding Missense Mutations in Mendelian Rare Diseases: Clues from Structural Bioinformatics" International Journal of Molecular Sciences 26, no. 9: 4072.
https://doi.org/10.3390/ijms26094072
APA Style
Visibelli, A., Finetti, R., Niccolai, P., Trezza, A., Spiga, O., Santucci, A., & Niccolai, N.
(2025). Profiling of Protein-Coding Missense Mutations in Mendelian Rare Diseases: Clues from Structural Bioinformatics. International Journal of Molecular Sciences, 26(9), 4072.
https://doi.org/10.3390/ijms26094072