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Journal Article
Blood, ISSN 1528-0020, 08/2006, Volume 108, Issue 4, pp. 1267 - 1279
Journal Article
Clinical kidney journal, ISSN 2048-8505, 2015, Volume 8, Issue 6, pp. 695 - 697
.... In this report, we discuss the case of a heterozygous carrier of a mutation on both factor H and membrane cofactor protein, who persistently presents haemolytic anaemia without need for blood... 
Membrane cofactor protein | Atypical haemolytic uraemic syndrome | Protein factor H | atypical haemolytic uraemic syndrome | Contents | protein factor H | membrane cofactor protein
Journal Article
The Lancet (British edition), ISSN 0140-6736, 2003, Volume 362, Issue 9395, pp. 1542 - 1547
.... We screened genes that encode the complement regulatory proteins—ie, factor H related 5, complement receptor 1, and membrane cofactor protein (MCP... 
Medicine, General & Internal | Life Sciences & Biomedicine | General & Internal Medicine | Science & Technology | Humans | Kidney Glomerulus - physiopathology | Male | Antigens, CD - genetics | Hemolytic-Uremic Syndrome - epidemiology | Membrane Glycoproteins - genetics | Polymerase Chain Reaction - methods | Polymorphism, Single-Stranded Conformational | Hemolytic-Uremic Syndrome - genetics | Complement System Proteins - physiology | Hemolytic-Uremic Syndrome - physiopathology | Pedigree | Adolescent | Age of Onset | Receptors, Complement - genetics | Adult | Complement System Proteins - genetics | Female | Membrane Cofactor Protein | Mutation | Complement Factor H - genetics | Complement Inactivator Proteins - genetics | Genetic aspects | Research | Gene mutations | Analysis | Hemolytic-uremic syndrome | Medical research | Disease | Patients | Genes | Pediatrics | Plasma | Complement receptors | Nephrology | Shiga toxin | Laboratories | Pathogenesis | Insertion | Complement | Gene polymorphism | Cell surface | Proteins | Genetic abnormalities | Complement factor H | Thrombotic thrombocytopenic purpura | Research centers | Deoxyribonucleic acid--DNA | Blood & organ donations | Abnormalities | Diarrhea | Complement regulatory proteins | Endothelial cells | Membrane proteins | Children & youth | Studies | Thrombocytopenic purpura | Complement activation | Hospitals | Purpura | Complement component C3 | Membrane cofactor protein | Protein expression | Microvasculature | Protein structure | Polymorphism | Index Medicus | Abridged Index Medicus
Journal Article