Thrombotic microangiopathy in aHUS and beyond: clinical clues from complement genetics
Author:
Publisher
Springer Science and Business Media LLC
Subject
Nephrology
Link
http://www.nature.com/articles/s41581-021-00424-4.pdf
Reference91 articles.
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2. Warwicker, P. et al. Familial relapsing haemolytic uraemic syndrome and complement factor H deficiency. Nephrol. Dial. Transpl. 14, 1229–1233 (1999).
3. Richards, A. et al. Mutations in human complement regulator, membrane cofactor protein (CD46), predispose to development of familial hemolytic uremic syndrome. Proc. Natl Acad. Sci. USA 100, 12966–12971 (2003).
4. Noris, M. et al. Familial haemolytic uraemic syndrome and an MCP mutation. Lancet 362, 1542–1547 (2003).
5. Fremeaux-Bacchi, V. et al. The development of atypical haemolytic-uraemic syndrome is influenced by susceptibility factors in factor H and membrane cofactor protein: evidence from two independent cohorts. J. Med. Genet. 42, 852–856 (2005).
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