The FXII c.-4T>C Polymorphism as a Disease Modifier in Patients With Hereditary Angioedema Due to the FXII p.Thr328Lys Variant-Reference-Cited by-同舟云学术

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

Published:2020-09-10 Issue: Volume:11 Page:
ISSN:1664-8021
Container-title:Frontiers in Genetics
language:
Short-container-title:Front. Genet.

Author:

Corvillo Fernando,Morena-Barrio María Eugenia de la,Marcos-Bravo Carmen,López-Trascasa Margarita,Vicente Vicente,Emsley Jonas,Caballero Teresa,Corral Javier,López-Lera Alberto

Publisher

Frontiers Media SA

Subject

Genetics(clinical),Genetics,Molecular Medicine

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4. Less severe clinical manifestations in patients with hereditary angioedema with missense C1INH gene mutations.;Bors;J. Allergy Clin. Immunol.,2013

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3. In Silico Analysis and In-depth Assessment of a Female Patient with a Missense Mutation in the F12 Gene Associated with Hereditary Angioedema Symptoms: A Case Study;2023-10-04

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