Martínez-Barricarte, R., Heurich, M., Valdes-Cañedo, F., Vazquez-Martul, E., Torreira, E., Montes, T., . . . Rodríguez de Córdoba, S. (2010). Human C3 mutation reveals a mechanism of dense deposit disease pathogenesis and provides insights into complement activation and regulation. American Society for Clinical Investigation.
Chicago-стиль цитированияMartínez-Barricarte, Rubén, et al. Human C3 Mutation Reveals a Mechanism of Dense Deposit Disease Pathogenesis and Provides Insights Into Complement Activation and Regulation. American Society for Clinical Investigation, 2010.
MLA-цитированиеMartínez-Barricarte, Rubén, et al. Human C3 Mutation Reveals a Mechanism of Dense Deposit Disease Pathogenesis and Provides Insights Into Complement Activation and Regulation. American Society for Clinical Investigation, 2010.