Tracing a Rare Genetic Disease: Familial Congenital CD59 Deficiency and Carrier Cases Identified through Village Screening: Erratum.


Kökcü Karadağ Ş. L., Alparslan M. K., Karadağ H., Turgut Uğurtay E., Can C., Yildiran A.

Journal of pediatric hematology/oncology, cilt.47, sa.5, 2025 (SCI-Expanded, Scopus) identifier identifier