Fištrek Prlić, M., Ćorić, M., Calabresi, L., Pavanello, C., Mosca, L., Cavallari, U. ... Jelaković, B. (2022). Two novel variants in the lecithin: cholesterol acyltransferase gene resulted in classic LCAT deficiency. Atherosclerosis Plus, 49., 28-31. doi: 10.1016/j.athplu.2022.05.005
Fištrek Prlić, Margareta, et al. "Two novel variants in the lecithin: cholesterol acyltransferase gene resulted in classic LCAT deficiency." Atherosclerosis Plus, vol. 49, 2022, pp. 28-31. https://doi.org/10.1016/j.athplu.2022.05.005
Fištrek Prlić, Margareta, Marijana Ćorić, Laura Calabresi, Chiara Pavanello, Lorena Mosca, Ugo Cavallari, Ivana Vuković Brinar, Sandra Karanović, Mario Laganović and Bojan Jelaković. "Two novel variants in the lecithin: cholesterol acyltransferase gene resulted in classic LCAT deficiency." Atherosclerosis Plus 49 (2022): 28-31. https://doi.org/10.1016/j.athplu.2022.05.005
Fištrek Prlić, M., et al. (2022) 'Two novel variants in the lecithin: cholesterol acyltransferase gene resulted in classic LCAT deficiency', Atherosclerosis Plus, 49, pp. 28-31. doi: 10.1016/j.athplu.2022.05.005
Fištrek Prlić M, Ćorić M, Calabresi L, Pavanello C, Mosca L, Cavallari U, and sur.. Two novel variants in the lecithin: cholesterol acyltransferase gene resulted in classic LCAT deficiency. Atherosclerosis Plus [Internet]. 2022 August [cited 2024 September 01];49:28-31. doi: 10.1016/j.athplu.2022.05.005
M. Fištrek Prlić, et al., "Two novel variants in the lecithin: cholesterol acyltransferase gene resulted in classic LCAT deficiency", Atherosclerosis Plus, vol. 49, pp. 28-31, August 2022. [Online]. Available at: https://urn.nsk.hr/urn:nbn:hr:105:605940. [Accessed: 01 September 2024]