Effect of Hereditary Hemochromatosis Gene H63D and C282Y Mutations on Iron Overload in Sickle Cell Disease Patients - Terzi, Yunus Kasım; Bulakbaşı Balcı, Tuğçe; Boğa, Can; Koç, Zafer; Yılmaz Çelik, Zerrin; Özdoğu, Hakan; Karakuş, Sema; İffet Şahin, Feride (Turkish journal of haematology, 2016)
Keywords: Adult; Alleles; Amino Acid Substitution; Anemia, Sickle Cell - complications; Anemia, Sickle Cell - diagnosis; Anemia, Sickle Cell - genetics; Biomarkers; Codon; Cross-Sectional Studies; DNA Mutational Analysis; Female; Gene Frequency; Genotype; hemochromatosis; Hemochromatosis Protein - genetics; Hemoglobin, Sickle - genetics; hfe gene; Homozygote; Humans; iron overload; Iron Overload - diagnosis; Iron Overload - etiology; Liver - metabolism; Liver - pathology; Magnetic Resonance Imaging; Male; Mutation; p.c282y; p.h63d; Prospective Studies; sickle cell anemia; Young Adult