Piras, R., Iatropoulos, P., Bresin, E., Todeschini, M., Gastoldi, S., Valoti, E., . . . Noris, M. (2020). Molecular Studies and an ex vivo Complement Assay on Endothelium Highlight the Genetic Complexity of Atypical Hemolytic Uremic Syndrome: The Case of a Pedigree With a Null CD46 Variant. Front Med (Lausanne).
Chicago-стиль цитированияPiras, Rossella, et al. "Molecular Studies and an Ex Vivo Complement Assay On Endothelium Highlight the Genetic Complexity of Atypical Hemolytic Uremic Syndrome: The Case of a Pedigree With a Null CD46 Variant." Front Med (Lausanne) 2020.
MLA-цитированиеPiras, Rossella, et al. "Molecular Studies and an Ex Vivo Complement Assay On Endothelium Highlight the Genetic Complexity of Atypical Hemolytic Uremic Syndrome: The Case of a Pedigree With a Null CD46 Variant." Front Med (Lausanne) 2020.