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Complement factor H deficiency and endocapillary glomerulonephritis due to paternal isodisomy and a novel factor H mutation

✍ Scribed by Schejbel, L; Schmidt, I M; Kirchhoff, M; Andersen, C B; Marquart, H V; Zipfel, P; Garred, P

Book ID: 109854990
Publisher: Nature Publishing Group
Year: 2011
Tongue: English
Weight: 559 KB
Volume: 12
Category: Article
ISSN: 1466-4879
DOI: 10.1038/gene.2010.63

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