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

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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PID : unige:137970
DOI : 10.1016/j.thromres.2019.08.012
PMID : 31479941

Additional URL for this publicationhttps://www.sciencedirect.com/science/article/pii/S0049384819303421

Journal ISSN0049-3848

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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.

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