Genetic and clinical characterization of congenital fibrinogen disorders in Polish patients: Identification of three novel fibrinogen gamma chain mutations-Reference-Cited by-同舟云学术

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

Published:2019-10 Issue: Volume:182 Page:133-140
ISSN:0049-3848
Container-title:Thrombosis Research
language:en
Short-container-title:Thrombosis Research

Author:

Wypasek Ewa,Klukowska Anna,Zdziarska Joanna,Zawilska Krystyna,Treliński Jacek,Iwaniec Teresa,Mital Andrzej,Pietrys Danuta,Sydor Wojciech,Neerman-Arbez Marguerite,Undas Anetta

Funder

Swiss National Science Foundation

Jagiellonian University Medical College

Publisher

Elsevier BV

Subject

Hematology

Reference41 articles.

1. Clinical consequences and molecular bases of low fibrinogen levels;Neerman-Arbez;Int. J. Mol. Sci.,2018

2. Diagnosis and classification of congenital fibrinogen disorders: communication from the SSC of the ISTH;Casini;J. Thromb. Haemost.,2018

3. clinical features and management of congenital fibrinogen deficiencies;Casini;Semin. Thromb. Hemost.,2016

4. Thromboembolism in patients with congenital afibrinogenaemia. Long-term observational data and systematic review;Nagler;Thromb. Haemost.,2016

5. Mutations in the fibrinogen alpha gene account for the majority of cases of congenital afibrinogenemia;Neerman-Arbez;Blood,2000

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