The FXII c.-4T>C Polymorphism as a Disease Modifier in Patients With Hereditary Angioedema Due to the FXII p.Thr328Lys Variant

Overview of attention for article published in Frontiers in Genetics, September 2020

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#PubSaludMurcia The FXII c.-4T>C Polymorphism as a Disease Modifier in Patients With Hereditary Angioedema Due to the FXII p.Thr328Lys Variant https://t.co/dVRh9eW5dk

04 Nov 2020

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New Research: The FXII c.-4T>C Polymorphism as a Disease Modifier in Patients With Hereditary Angioedema Due to the FXII p.Thr328Lys Variant: Background Hereditary angioedema due to the Thr328Lys variant in the coagulation factor XII (HAE-FXII)… https:/

10 Oct 2020

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