Genotype-phenotype analyses of Iranian patients with hemophilia B (Leyden -) and hemophilia B (Leyden +): A single-center study.
Arash Ahmadfard MoghadamAmir Reza ManafzadehKhadijeh DajliryFarahnaz RamezanMohammad Reza NikooniaBabak AbdolkarimiMohsen HamidpourShadi TabibianPublished in: Transfusion and apheresis science : official journal of the World Apheresis Association : official journal of the European Society for Haemapheresis (2024)
The results of this study confirm that HB is caused by a wide range of molecular defects in Iran. Thus, by knowing the genotypes and phenotypes, we would be able to stratify the patients which is important in terms of their management and outcome.