Membranous nephropathy in a patient with hereditary complete complement C4 deficiency
Nephrol Dial Transplant
.
2004 Apr;19(4):990-3.
doi: 10.1093/ndt/gfh008.
Authors
Karl Lhotta
1
,
Reinhard Würzner
,
Hans J Rumpelt
,
Paula Eder
,
Gert Mayer
Affiliation
1
Division of Clinical Nephrology, Department of Internal Medicine, Innsbruck University Hospital, Anichstrasse 35, A-6020 Innsbruck, Austria. karl.lhotta@uibk.ac.at
PMID:
15031363
DOI:
10.1093/ndt/gfh008
No abstract available
Publication types
Case Reports
MeSH terms
Adolescent
Child
Complement C4 / deficiency*
Follow-Up Studies
Glomerulonephritis, Membranous / etiology*
Humans
Male
Substances
Complement C4