Genetic and clinical characterization of congenital fibrinogen disorders in Polish patients: Identification of three novel fibrinogen gamma chain mutations

Congenital fibrinogen disorders are poorly explored in Slavic populations. The aim of this study was to characterize the genetic background and clinical manifestations of fibrinogen disorders in the Polish case series.

Source: Thrombosis Research - August 23, 2019 Category: Hematology Authors: Ewa Wypasek, Anna Klukowska, Joanna Zdziarska, Krystyna Zawilska, Jacek Treli ński, Teresa Iwaniec, Andrzej Mital, Danuta Pietrys, Wojciech Sydor, Marguerite Neerman-Arbez, Anetta Undas Tags: Full Length Article Source Type: research