A. Tortajada Et Al. , "Complement factor H variants I890 and L1007 while commonly associated with atypical hemolytic uremic syndrome are polymorphisms with no functional significance," KIDNEY INTERNATIONAL , vol.81, no.1, pp.56-63, 2012
Tortajada, A. Et Al. 2012. Complement factor H variants I890 and L1007 while commonly associated with atypical hemolytic uremic syndrome are polymorphisms with no functional significance. KIDNEY INTERNATIONAL , vol.81, no.1 , 56-63.
Tortajada, A., Pinto, S., Martinez-Ara, J., Lopez-Trascasa, M., Sanchez-Corral, P., & Rodriguez de Cordoba, S., (2012). Complement factor H variants I890 and L1007 while commonly associated with atypical hemolytic uremic syndrome are polymorphisms with no functional significance. KIDNEY INTERNATIONAL , vol.81, no.1, 56-63.
Tortajada, Agustin Et Al. "Complement factor H variants I890 and L1007 while commonly associated with atypical hemolytic uremic syndrome are polymorphisms with no functional significance," KIDNEY INTERNATIONAL , vol.81, no.1, 56-63, 2012
Tortajada, Agustin Et Al. "Complement factor H variants I890 and L1007 while commonly associated with atypical hemolytic uremic syndrome are polymorphisms with no functional significance." KIDNEY INTERNATIONAL , vol.81, no.1, pp.56-63, 2012
Tortajada, A. Et Al. (2012) . "Complement factor H variants I890 and L1007 while commonly associated with atypical hemolytic uremic syndrome are polymorphisms with no functional significance." KIDNEY INTERNATIONAL , vol.81, no.1, pp.56-63.
@article{article, author={Agustin Tortajada Et Al. }, title={Complement factor H variants I890 and L1007 while commonly associated with atypical hemolytic uremic syndrome are polymorphisms with no functional significance}, journal={KIDNEY INTERNATIONAL}, year=2012, pages={56-63} }