Ozen, A.; Kasap, N.; Vujkovic-Cvijin, I.; Apps, R.; Cheung, F.; Karakoc-Aydiner, E.; Akkelle, B.; Sari, S.; Tutar, E.; Ozcay, F.; Uygun, D.K.; Islek, A.; Akgun, G.; Selcuk, M.; Sezer, O.B.; Zhang, Y.; Kutluk, G.; Topal, E.; Sayar, E.; Celikel, C.; Houwen, R.H.J.; Bingol, A.; Ogulur, I.; Eltan, S.B.; Snow, A.L.; Lake, C.; Fantoni, G.; Alba, C.; Sellers, B.; Chauvin, S.D.; Dalgard, C.L.; Harari, O.; Ni, Y.G.; Wang, M.-D.; Devalaraja-Narashimha, K.; Subramanian, P.; Ergelen, R.; Artan, R.; Guner, S.N.; Dalgic, B.; Tsang, J.; Belkaid, Y.; Ertem, D.; Baris, S.; Lenardo, M.J.
(2021)
Complement hyperactivation, angiopathic thrombosis and protein-losing enteropathy (CHAPLE disease) is a lethal disease caused by genetic loss of the complement regulatory protein CD55, leading to overactivation of complement ...