On the relevance of thrombomodulin variants in atypical hemolytic uremic syndrome

Atypical hemolytic uremic syndrome; Genetic analysis; ThrombomodulinSíndrome hemolítica urèmica atípica; Anàlisi genètica; TrombomodulinaSíndrome hemolítico urémico atípico; Análisis genético; TrombomodulinaThis project was funded by the Instituto de Salud Carlos III: REDinREN (RD016/009/009) and Instituto de Investigacion Puerta de Hierro-Segovia Arana (IDIPHISA) to AH and by grants from the Spanish Ministerio de Economía y Competitividad–FEDER (European Regional Development Fund) (PID2019-104912RB-I00) and the Autonomous Region of Madrid (S2017/BMD-3673 and S2022/BMD-7278) to SRdC. TC was supported by a grant from National Health Institute Carlos III (RETIC ISCIII RD21/0005; RICORS), This work was developed under the supervision of the Spanish Registry of the Atypical Hemolytic Uremic Syndrome and C3 Glomerulopathy (aHUS/C3G) registry