Biallelic mutations in the CFHR genes underlying atypical hemolytic uremic syndrome in a patient with catastrophic adult-onset Still's disease and recurrent macrophage activation syndrome: A case report
Titel:
Biallelic mutations in the CFHR genes underlying atypical hemolytic uremic syndrome in a patient with catastrophic adult-onset Still's disease and recurrent macrophage activation syndrome: A case report
Auteur:
Dillemans, Luna Bekhuis, Youri Betrains, Albrecht Yu, Karen van Hemelen, Maarten Pörtner, Noëmie De Somer, Lien Matthys, Patrick Breckpot, Jeroen Tousseyn, Thomas Peetermans, Marijke Proost, Paul Wouters, Carine Vanderschueren, Steven