Human C3 mutation reveals a mechanism of dense deposit disease pathogenesis and provides insights into complement activation and regulation

1. Martínez-Barricarte, R.
2. Heurich, M.
3. Valdes-Cañedo, F.
4. Vazquez-Martul, E.
5. Torreira, E.
6. Montes, T.
7. Tortajada, A.
8. Pinto, S.
9. Lopez-Trascasa, M.
10. Morgan, B.P.
11. Llorca, O.
12. Harris, C.L.
13. De Córdoba, S.R.