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Sefika Ilknur KK, Medine KA, Huseyin K, Eda Turgut U, et al. Tracing a Rare Genetic Disease: Familial Congenital CD59 Deficiency and Carrier Cases Identified Through Village Screening. J Pediatr Hematol Oncol 2025;47:109-114.
PMID: 40126046


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