Deletion of Complement Factor H–Related Genes CFHR1 and CFHR3 Is Associated with Atypical Hemolytic Uremic Syndrome

Atypical hemolytic uremic syndrome (aHUS) is associated with defective complement regulation. Disease-associated mutations have been described in the genes encoding the complement regulators complement factor H, membrane cofactor protein, factor B, and factor I. In this study, we show in two indepen...

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Detalles Bibliográficos
Autores principales: Zipfel, Peter F, Edey, Matthew, Heinen, Stefan, Józsi, Mihály, Richter, Heiko, Misselwitz, Joachim, Hoppe, Bernd, Routledge, Danny, Strain, Lisa, Hughes, Anne E, Goodship, Judith A, Licht, Christoph, Goodship, Timothy H. J, Skerka, Christine
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2007
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1828695/
https://www.ncbi.nlm.nih.gov/pubmed/17367211
http://dx.doi.org/10.1371/journal.pgen.0030041

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1828695/
https://www.ncbi.nlm.nih.gov/pubmed/17367211
http://dx.doi.org/10.1371/journal.pgen.0030041

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