Dellepiane, R.M.; Baselli, L.A.; Cazzaniga, M.; Lougaris, V.; Macor, P.; Giordano, M.; Gualtierotti, R.; Cugno, M.
Hereditary Deficiency of the Second Component of Complement: Early Diagnosis and 21-Year Follow-Up of a Family. Medicina 2020, 56, 120.
https://doi.org/10.3390/medicina56030120
AMA Style
Dellepiane RM, Baselli LA, Cazzaniga M, Lougaris V, Macor P, Giordano M, Gualtierotti R, Cugno M.
Hereditary Deficiency of the Second Component of Complement: Early Diagnosis and 21-Year Follow-Up of a Family. Medicina. 2020; 56(3):120.
https://doi.org/10.3390/medicina56030120
Chicago/Turabian Style
Dellepiane, Rosa Maria, Lucia Augusta Baselli, Marco Cazzaniga, Vassilios Lougaris, Paolo Macor, Mara Giordano, Roberta Gualtierotti, and Massimo Cugno.
2020. "Hereditary Deficiency of the Second Component of Complement: Early Diagnosis and 21-Year Follow-Up of a Family" Medicina 56, no. 3: 120.
https://doi.org/10.3390/medicina56030120
APA Style
Dellepiane, R. M., Baselli, L. A., Cazzaniga, M., Lougaris, V., Macor, P., Giordano, M., Gualtierotti, R., & Cugno, M.
(2020). Hereditary Deficiency of the Second Component of Complement: Early Diagnosis and 21-Year Follow-Up of a Family. Medicina, 56(3), 120.
https://doi.org/10.3390/medicina56030120