Galatolo, D.; De Michele, G.; Silvestri, G.; Leuzzi, V.; Casali, C.; Musumeci, O.; Antenora, A.; Astrea, G.; Barghigiani, M.; Battini, R.;
et al. NGS in Hereditary Ataxia: When Rare Becomes Frequent. Int. J. Mol. Sci. 2021, 22, 8490.
https://doi.org/10.3390/ijms22168490
AMA Style
Galatolo D, De Michele G, Silvestri G, Leuzzi V, Casali C, Musumeci O, Antenora A, Astrea G, Barghigiani M, Battini R,
et al. NGS in Hereditary Ataxia: When Rare Becomes Frequent. International Journal of Molecular Sciences. 2021; 22(16):8490.
https://doi.org/10.3390/ijms22168490
Chicago/Turabian Style
Galatolo, Daniele, Giovanna De Michele, Gabriella Silvestri, Vincenzo Leuzzi, Carlo Casali, Olimpia Musumeci, Antonella Antenora, Guja Astrea, Melissa Barghigiani, Roberta Battini,
and et al. 2021. "NGS in Hereditary Ataxia: When Rare Becomes Frequent" International Journal of Molecular Sciences 22, no. 16: 8490.
https://doi.org/10.3390/ijms22168490
APA Style
Galatolo, D., De Michele, G., Silvestri, G., Leuzzi, V., Casali, C., Musumeci, O., Antenora, A., Astrea, G., Barghigiani, M., Battini, R., Battisti, C., Caputi, C., Cioffi, E., De Michele, G., Dotti, M. T., Fico, T., Fiorillo, C., Galosi, S., Lieto, M.,
... Santorelli, F. M.
(2021). NGS in Hereditary Ataxia: When Rare Becomes Frequent. International Journal of Molecular Sciences, 22(16), 8490.
https://doi.org/10.3390/ijms22168490