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Volumn 30, Issue 5, 2015, Pages 862-864
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Familial C3 glomerulonephritis associated with mutations in the gene for complement factor B
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Author keywords
C3 glomerulonephritis; complement alternative pathway; complement factor B; genetic mutation
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Indexed keywords
ALTERNATIVE COMPLEMENT PATHWAY C3 C5 CONVERTASE;
COMPLEMENT COMPONENT C3;
COMPLEMENT COMPONENT C4;
COMPLEMENT MEMBRANE ATTACK COMPLEX;
CYCLOSPORIN;
STEROID;
ARTICLE;
C3 GLOMERULONEPHRITIS;
CASE REPORT;
CHILD;
COMPLEMENT FACTOR B GENE;
CONTROLLED STUDY;
DNA DETERMINATION;
FEMALE;
GAIN OF FUNCTION MUTATION;
GENETIC ASSOCIATION;
GLOMERULONEPHRITIS;
HEMATURIA;
HETEROZYGOSITY;
HUMAN;
HUMAN TISSUE;
KIDNEY BIOPSY;
MEDICAL HISTORY;
MEMBRANOPROLIFERATIVE GLOMERULONEPHRITIS;
PHYSICAL EXAMINATION;
PRIORITY JOURNAL;
PROTEINURIA;
SCHOOL CHILD;
ADOLESCENT;
BIOPSY;
FAMILY HEALTH;
GENETICS;
HETEROZYGOTE;
KIDNEY;
MALE;
MIDDLE AGED;
MUTATION;
NUCLEOTIDE SEQUENCE;
PATHOLOGY;
ADOLESCENT;
BIOPSY;
CHILD;
COMPLEMENT FACTOR B;
DNA MUTATIONAL ANALYSIS;
FAMILY HEALTH;
FEMALE;
GLOMERULONEPHRITIS;
GLOMERULONEPHRITIS, MEMBRANOPROLIFERATIVE;
HEMATURIA;
HETEROZYGOTE;
HUMANS;
KIDNEY;
MALE;
MIDDLE AGED;
MUTATION;
PROTEINURIA;
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EID: 84929583971
PISSN: 09310509
EISSN: 14602385
Source Type: Journal
DOI: 10.1093/ndt/gfv054 Document Type: Article |
Times cited : (21)
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References (10)
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