Cite
Analysis of LPI-causing mutations on y+LAT1 function and localization.
MLA
Rotoli, Bianca Maria, et al. “Analysis of LPI-Causing Mutations on Y+LAT1 Function and Localization.” Orphanet Journal of Rare Diseases, vol. 14, no. 1, Mar. 2019, p. N.PAG. EBSCOhost, https://doi.org/10.1186/s13023-019-1028-2.
APA
Rotoli, B. M., Barilli, A., Ingoglia, F., Visigalli, R., Bianchi, M. G., Ferrari, F., Martinelli, D., Dionisi-Vici, C., & Dall’Asta, V. (2019). Analysis of LPI-causing mutations on y+LAT1 function and localization. Orphanet Journal of Rare Diseases, 14(1), N.PAG. https://doi.org/10.1186/s13023-019-1028-2
Chicago
Rotoli, Bianca Maria, Amelia Barilli, Filippo Ingoglia, Rossana Visigalli, Massimiliano G. Bianchi, Francesca Ferrari, Diego Martinelli, Carlo Dionisi-Vici, and Valeria Dall’Asta. 2019. “Analysis of LPI-Causing Mutations on Y+LAT1 Function and Localization.” Orphanet Journal of Rare Diseases 14 (1): N.PAG. doi:10.1186/s13023-019-1028-2.