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).
Citación estilo ChicagoPiras, 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.
Cita MLAPiras, 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.