Characterization of a factor H mutation that perturbs the alternative pathway of complement in a family with membranoproliferative GN. [electronic resource]
Producer: 20150105Description: 2425-33 p. digitalISSN:- 1533-3450
- Animals
- Complement Factor H -- chemistry
- Complement Pathway, Alternative -- genetics
- Crystallography, X-Ray
- Erythrocytes -- cytology
- Family Health
- Female
- Glomerulonephritis, Membranoproliferative -- genetics
- Haplotypes
- Hereditary Complement Deficiency Diseases
- Heterozygote
- Humans
- Kidney Diseases -- genetics
- Male
- Pedigree
- Polymorphism, Genetic
- Protein Structure, Tertiary
- Sheep
- Structure-Activity Relationship
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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