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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.

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Dades bibliogràfiques
Autors principals: Noris, Marina, Remuzzi, Giuseppe
Format: Artigo
Idioma:Inglês
Publicat: Public Library of Science 2006
Matèries:
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC1626557/
https://ncbi.nlm.nih.gov/pubmed/17076562
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pmed.0030432
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