Combined complement gene mutations in atypical hemolytic uremic syndrome influence clinical phenotype. [electronic resource]
Producer: 20130424Description: 475-86 p. digitalISSN:- 1533-3450
- Adult
- Atypical Hemolytic Uremic Syndrome
- Child
- Child, Preschool
- Complement C3 -- genetics
- Complement Factor B -- genetics
- Complement Factor H -- genetics
- Complement System Proteins -- genetics
- Female
- Fibrinogen -- genetics
- Genetic Association Studies
- Haplotypes
- Hemolytic-Uremic Syndrome -- genetics
- Humans
- Infant
- Male
- Membrane Cofactor Protein -- genetics
- Middle Aged
- Mutation
- Pedigree
- Penetrance
- Risk Factors
- Young Adult
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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