Complement Factor H Gene Abnormalities in Haemolytic Uraemic Syndrome: From Point Mutations to Hybrid Gene

Noris and Remuzzi discuss a new study showing an association between atypical haemolytic uremic syndrome and a hybrid complement gene,CFH/CFHL1.

Detalles Bibliográficos
Autores principales: Noris, Marina, Remuzzi, Giuseppe
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2006
Materias:
Perspectives
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1626557/
https://www.ncbi.nlm.nih.gov/pubmed/17076562
http://dx.doi.org/10.1371/journal.pmed.0030432

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1626557/
https://www.ncbi.nlm.nih.gov/pubmed/17076562
http://dx.doi.org/10.1371/journal.pmed.0030432

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