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

Published inThrombosis Research, vol. 182, p. 133-140
Publication date2019
Abstract

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.

Citation (ISO format)
WYPASEK, Ewa et al. Genetic and clinical characterization of congenital fibrinogen disorders in polish patients: identification of three novel fibrinogen gamma chain mutations. In: Thrombosis Research, 2019, vol. 182, p. 133–140. doi: 10.1016/j.thromres.2019.08.012
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ISSN of the journal0049-3848
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