Screening for Plasminogen Mutations in Hereditary Angioedema Patients
Hereditary angioedema (HAE) is a rare disease belonging to the group of bradykinin-mediated angioedemas, characterized by recurring edematous episodes involving the subcutaneous and/or submucosal tissues. Most cases of HAE are caused by mutations in the <i>SERPING1</i> gene encoding C1-i...
Main Authors: | Henriette Farkas, Anna Dóczy, Edina Szabó, Lilian Varga, Dorottya Csuka |
---|---|
Format: | Article |
Language: | English |
Published: |
MDPI AG
2021-03-01
|
Series: | Genes |
Subjects: | |
Online Access: | https://www.mdpi.com/2073-4425/12/3/402 |
Similar Items
-
Treatment of patients with hereditary angioedema with the c.988A>G (p.Lys330Glu) variant in the plasminogen gene
by: Konrad Bork, et al.
Published: (2020-02-01) -
Commentary: Bradykinin-Mediated Angioedema: An Update of the Genetic Causes and the Impact of Genomics
by: Roger Colobran, et al.
Published: (2020-04-01) -
Genotype-first analysis of a generally healthy population cohort supports genetic testing for diagnosis of hereditary angioedema of unknown cause
by: Dale L. Bodian, et al.
Published: (2019-05-01) -
Hereditary angioedema
by: Helen Lesser, et al.
Published: (2021-07-01) -
Hereditary Angioedema
by: A.P. Volokha
Published: (2014-03-01)