Search Results - "MsC, Caty Carrerra"
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Exome Sequencing and Clot Lysis Experiments Demonstrate the R458C Mutation of the Alpha Chain of Fibrinogen to be Associated with Impaired Fibrinolysis in a Family with Thrombophilia
Published in Journal of Atherosclerosis and Thrombosis (01-01-2016)“…Aim: We report the study of a familial rare disease with recurrent venous thromboembolic events that remained undiagnosed for many years using standard…”
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Journal Article -
2
Exome Sequencing and Clot Lysis Experiments Demonstrate the R458C Mutation of the Alpha Chain of Fibrinogen to be Associated with Impaired Fibrinolysis in a Family with Thrombophilia
Published in Journal of Atherosclerosis and Thrombosis (2016)“…[Aim]: We report the study of a familial rare disease with recurrent venous thromboembolic events that remained undiagnosed for many years using standard…”
Get full text
Journal Article