Heterozygous FGA p.Asp473Ter (fibrinogen Nieuwegein) presenting as antepartum cerebral thrombosis-Reference-Cited by-同舟云学术

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Heterozygous FGA p.Asp473Ter (fibrinogen Nieuwegein) presenting as antepartum cerebral thrombosis

Published:2018-03 Issue: Volume:163 Page:185-189
ISSN:0049-3848
Container-title:Thrombosis Research
language:en
Short-container-title:Thrombosis Research

Author:

Tajdar Mercedeh^ORCID,Orlando Christelle,Casini Alessandro,Herpol Margaux,De Bisschop Barbara,Govaert Paul,Neerman-Arbez Marguerite,Jochmans Kristin

Publisher

Elsevier BV

Subject

Hematology

Reference29 articles.

1. Laboratory and genetic investigations of mutations accounting for congenital fibrinogen disorders;Neerman-Arbez;Semin. Thromb. Hemost.,2016

2. Congenital fibrinogen disorders: an update;de Moerloose;Semin. Thromb. Hemost.,2013

3. Aberrant fibrin formation and cross-linking of fibrinogen Nieuwegein, a variant with a shortened Aα-chain, alters endothelial capillary tube formation;Collen;Blood,2001

4. Molecular characterization of 7 patient affected by dys- or hypo-dysfibrinogenemia: identification of a novel mutation in the fibrinogen Bbeta chain causing a gain of glycosylation;Asselta;Thromb. Res.,2015

5. Evolution and organisation of the fibrinogen locus on chromosome 4: gene dublication accompanied by transposition and inversion;Kant;Proc. Natl. Acad. Sci. U. S. A.,1985

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2. Developmental anatomy of the thalamus, perinatal lesions, and neurological development;Developmental Medicine & Child Neurology;2024-06-14

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