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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Bibliografische gegevens
Hoofdauteurs: 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
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: Public Library of Science 2007
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Research Article
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC1828695/
https://ncbi.nlm.nih.gov/pubmed/17367211
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pgen.0030041
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