Complement factor h gene abnormalities in haemolytic uraemic syndrome: from point mutations to hybrid gene.
editorial · Level V
Where this comes from
- Record sourced from PubMed, PMID 17076562.
- Also identified by PMC identifier 1626557.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
Abstract
Noris and Remuzzi discuss a new study showing an association between atypical haemolytic uremic syndrome and a hybrid complement gene,<i>CFH/CFHL1.</i>
Medical subject headings
- Complement Factor H
- Hemolytic-Uremic Syndrome
- Mutant Chimeric Proteins
- Point Mutation