Aiello, M., Fantin, A., Longo, C., Ferrarotti, I., Bertorelli, G., & Chetta, A. (2020). Clinical manifestations in patients with PI*MMMalton genotypes. A matter still unsolved in alpha‐1 antitrypsin deficiency. Respirology Case Reports, 8(3), 1. https://doi.org/10.1002/rcr2.528
Chicago Style (17th ed.) CitationAiello, Marina, Alberto Fantin, Chiara Longo, Ilaria Ferrarotti, Giuseppina Bertorelli, and Alfredo Chetta. "Clinical Manifestations in Patients with PI*MMMalton Genotypes. A Matter Still Unsolved in Alpha‐1 Antitrypsin Deficiency." Respirology Case Reports 8, no. 3 (2020): 1. https://doi.org/10.1002/rcr2.528.
MLA (9th ed.) CitationAiello, Marina, et al. "Clinical Manifestations in Patients with PI*MMMalton Genotypes. A Matter Still Unsolved in Alpha‐1 Antitrypsin Deficiency." Respirology Case Reports, vol. 8, no. 3, 2020, p. 1, https://doi.org/10.1002/rcr2.528.