Hyperfunctional C3 convertase leads to complement deposition on endothelial cells and contributes to atypical hemolytic uremic syndrome. [electronic resource]
Producer: 20091027Description: 2837-45 p. digitalISSN:- 1528-0020
- Adolescent
- Adult
- Aged
- Aged, 80 and over
- Cells, Cultured
- Child
- Child, Preschool
- Cohort Studies
- Complement Activation -- genetics
- Complement C3-C5 Convertases -- genetics
- Complement System Proteins -- genetics
- Endothelial Cells -- metabolism
- Family
- Female
- Hemolytic-Uremic Syndrome -- genetics
- Humans
- Infant
- Infant, Newborn
- Male
- Middle Aged
- Models, Molecular
- Mutant Proteins -- physiology
- Pedigree
- Young Adult
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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