Molecular analysis of patients with severe congenital factor X deficiency: First report from north and northwest of Iran.

@article{Morovvati2015MolecularAO,
  title={Molecular analysis of patients with severe congenital factor X deficiency: First report from north and northwest of Iran.},
  author={Saeid Morovvati and Reza Ranjbar and Mohammadreza Younesi},
  journal={Hematology},
  year={2015}
}
Background Congenital FX deficiency is an extremely rare autosomal recessive disorder, mostly present in regions with a high rate of consanguinity, with an incidence of approximately 1:2,000,000 in the general population. The aim of this study was to evaluate the clinical manifestations and to provide a molecular analysis of 14 patients with homozygous… CONTINUE READING