MPGN II - genetically determined by defective complement regulation?
MPGN II is a rare disease which is characterized by complement containing deposits within the GBM. The disease is characterized by functional impairment of the GBM causing progressive loss of renal function eventually resulting in end stage renal disease.
Gespeichert in:
| Hauptverfasser: | , , , , |
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| Dokumenttyp: | Article (Journal) |
| Sprache: | Englisch |
| Veröffentlicht: |
2007
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| In: |
Pediatric nephrology
Year: 2007, Jahrgang: 22, Heft: 1, Pages: 2-9 |
| ISSN: | 1432-198X |
| DOI: | 10.1007/s00467-006-0299-8 |
| Online-Zugang: | Verlag, lizenzpflichtig, Volltext: https://dx.doi.org/10.1007/s00467-006-0299-8 Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1007/s00467-006-0299-8 
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| Verfasserangaben: | Christoph Licht, Ursula Schlötzer-Schrehardt, Michael Kirschfink, Peter F. Zipfel, Bernd Hoppe |
MARC
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