A hybrid CFHR3-1 gene causes familial C3 glomerulopathy

Journal of the American Society of Nephrology

Volumn 23, Issue 7, 2012, Pages 1155-1160

  Malik, Talat H ^a   Lavin, Peter J ^b,c   De Jorge, Elena Goicoechea ^a   Vernon, Katherine A ^a   Rose, Kirsten L ^a   Patel, Mitali P ^a   De Leeuw, Marcel ^d   Neary, John J ^e   Conlon, Peter J ^f   Winn, Michelle P ^b   Pickering, Matthew C ^a  

^a IMPERIAL COLLEGE LONDON   (United Kingdom)

^b DUKE UNIVERSITY MEDICAL CENTER   (United States)

^c ADELAIDE AND MEATH HOSPITAL   (Ireland)

^d BECKMAN COULTER INC   (United States)

^e ROYAL INFIRMARY OF EDINBURGH   (United Kingdom)

^f BEAUMONT HOSPITAL   (Ireland)

Author keywords

[No Author keywords available]

Indexed keywords

COMPLEMENT FACTOR H; COMPLEMENT FACTOR H RELATED PROTEIN[3-1]; UNCLASSIFIED DRUG;

ADULT; ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; CLINICAL ARTICLE; COMPLEMENT ACTIVATION; COMPLEMENT COMPONENT C3 MEDIATED GLOMERULOPATHY; COPY NUMBER VARIATION; DNA HYBRIDIZATION; FAMILIAL DISEASE; GENE DELETION; GENE LOCUS; GENE SEQUENCE; GENETIC ASSOCIATION; GLOMERULOPATHY; HUMAN; IMMUNOGLOBULIN A NEPHROPATHY; PRIORITY JOURNAL;

EID: 84863511490     PISSN: 10466673     EISSN: 15333450     Source Type: Journal    
DOI: 10.1681/ASN.2012020166     Document Type: Article

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