Secondary focal and segmental glomerulosclerosis associated with single-nucleotide polymorphisms in the genes encoding complement factor H and C3

American Journal of Kidney Diseases

Volumn 60, Issue 2, 2012, Pages 316-321

  Sethi, Sanjeev ^a   Fervenza, Fernando C ^a   Zhang, Yuzhou ^b   Smith, Richard J H ^b  

^a MAYO CLINIC   (United States)

^b UNIVERSITY OF IOWA   (United States)

Author keywords

alternative pathway of complement; C3; chronic thrombotic microangiopathy; factor H; Focal and segmental glomerulosclerosis (FSGS)

Indexed keywords

COMPLEMENT COMPONENT C3; COMPLEMENT FACTOR H;

ADULT; ARTICLE; CASE REPORT; COMPLEMENT ALTERNATIVE PATHWAY; DNA STRUCTURE; ELECTRON MICROSCOPY; FEMALE; FOCAL GLOMERULOSCLEROSIS; GENE MUTATION; GENETIC ASSOCIATION; GENETIC CODE; GENETIC POLYMORPHISM; GLOMERULOPATHY; GLOMERULUS CAPILLARY; HEMOLYTIC ANEMIA; HEREDITY; HISTOPATHOLOGY; HUMAN; IMMUNOFLUORESCENCE; KIDNEY BIOPSY; SINGLE NUCLEOTIDE POLYMORPHISM; THROMBOTIC THROMBOCYTOPENIC PURPURA;

COMPLEMENT C3; COMPLEMENT FACTOR H; COMPLEMENT PATHWAY, ALTERNATIVE; FEMALE; GLOMERULOSCLEROSIS, FOCAL SEGMENTAL; HUMANS; MIDDLE AGED; POLYMORPHISM, SINGLE NUCLEOTIDE; SEQUENCE ANALYSIS, PROTEIN;

EID: 84863981321     PISSN: 02726386     EISSN: 15236838     Source Type: Journal    
DOI: 10.1053/j.ajkd.2012.04.011     Document Type: Article

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