| Literature DB >> 35318588 |
Victor Milon1, Nicolas Fage1, Fanny Guibert1,2, Véronique Frémeaux-Bacchi3, Jean-François Augusto4, Benoit Brilland1.
Abstract
Entities:
Keywords: Hemolytic and uremic syndrome; MCP mutation; Thrombotic microangiopathy; Thrombotic thrombocytopenic purpura
Mesh:
Year: 2022 PMID: 35318588 DOI: 10.1007/s40620-022-01289-x
Source DB: PubMed Journal: J Nephrol ISSN: 1121-8428 Impact factor: 3.902