Factor H, membrane cofactor protein, and factor I mutations in patients with hemolysis, elevated liver enzymes, and low platelet count syndrome - Fakhouri, Fadi; Jablonski, Mathieu; Lepercq, Jacques; Blouin, Jacques; Benachi, Alexandra; Hourmant, Maryvonne; Pirson, Yves; Dürrbach, Antoine; Grünfeld, Jean-Pierre; Knebelmann, Bertrand; Frémeaux-Bacchi, Véronique (Blood, 2008)
Keywords: Adult; Biological and medical sciences; Complement Factor H - genetics; Complement System Proteins - genetics; DNA Mutational Analysis; Female; Fibrinogen - genetics; Genetic Predisposition to Disease; Gestational Age; HELLP Syndrome - genetics; Hematologic and hematopoietic diseases; Humans; Medical sciences; Membrane Cofactor Protein - genetics; Mutation, Missense; Other diseases. Hematologic involvement in other diseases; Pregnancy; Risk Factors; Young Adult; Kidney disease; Human; Immunopathology; Factor H; Urinary system disease; Serine endopeptidases; Enzyme; Alternative pathway complement; HELLP syndrome; Hemopathy; Immune deficiency; Complement Factor I; Peptidases; Acute renal insufficiency; Gene; Complement deficiency; Membrane cofactor protein; Genetics; Hydrolases; Complication; Mutation