Recessive mutations in DGKE cause atypical hemolytic-uremic syndrome-Reference-Cited by-同舟云学术

Recessive mutations in DGKE cause atypical hemolytic-uremic syndrome

Published:2013-03-31 Issue:5 Volume:45 Page:531-536
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Lemaire Mathieu,Frémeaux-Bacchi Véronique,Schaefer Franz,Choi Murim,Tang Wai Ho,Le Quintrec Moglie,Fakhouri Fadi,Taque Sophie,Nobili François,Martinez Frank,Ji Weizhen,Overton John D,Mane Shrikant M,Nürnberg Gudrun,Altmüller Janine,Thiele Holger,Morin Denis,Deschenes Georges,Baudouin Véronique,Llanas Brigitte,Collard Laure,Majid Mohammed A,Simkova Eva,Nürnberg Peter,Rioux-Leclerc Nathalie,Moeckel Gilbert W,Gubler Marie Claire,Hwa John,Loirat Chantal,Lifton Richard P

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng.2590.pdf

Reference46 articles.

1. Neild, G.H. Haemolytic-uraemic syndrome in practice. Lancet 343, 398–401 (1994).

2. Loirat, C. & Frémeaux-Bacchi, V. Atypical hemolytic uremic syndrome. Orphanet J. Rare Dis. 6, 60 (2011).

3. Noris, M., Mescia, F. & Remuzzi, G. STEC-HUS, atypical HUS and TTP are all diseases of complement activation. Nat. Rev. Nephrol. 8, 622–633 (2012).

4. Noris, M. & Remuzzi, G. Atypical hemolytic-uremic syndrome. N. Engl. J. Med. 361, 1676–1687 (2009).

5. Zuber, J., Fakhouri, F., Roumenina, L.T., Loirat, C. & Frémeaux-Bacchi, V. Use of eculizumab for atypical haemolytic uraemic syndrome and C3 glomerulopathies. Nat. Rev. Nephrol. 8, 643–657 (2012).

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