Congenital afibrinogenemia: intracellular retention of fibrinogen due to a novel W437G mutation in the fibrinogen Bβ-chain gene
Author:
Publisher
Elsevier BV
Subject
Molecular Biology,Molecular Medicine
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1. Molecular and clinical profile of congenital fibrinogen disorders in Iran, identification of two novel mutations;International Journal of Laboratory Hematology;2020-07-08
2. Congenital afibrinogenemia: Identification and characterization of two novel homozygous fibrinogen Aα and Bβ chain mutations in two Tunisian families;Thrombosis Research;2016-07
3. FGB mutations leading to congenital quantitative fibrinogen deficiencies: An update and report of four novel mutations;Thrombosis Research;2014-05
4. A novel fibrinogen B beta chain frameshift mutation causes congenital afibrinogenaemia;Thrombosis and Haemostasis;2013
5. Manipulating the quality control pathway in transfected cells: low temperature allows rescue of secretion-defective fibrinogen mutants;Haematologica;2008-02-01
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