Innovations in Hereditary Angioedema Pathophysiology
Hereditary angioedema (HAE) is a rare, inherited disease mostly associated with mutations in the SERPING1 gene (serpin family G member 1), which encodes the C1 inhibitor (C1-INH) protein. Regulation can lead to plasma deficiency and ensuing repeated attacks of severe angioedema. This disease was fir...
| Main Author: | |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
KARE Publishing
2019-12-01
|
| Series: | Southern Clinics of Istanbul Eurasia |
| Subjects: | |
| Online Access: | https://jag.journalagent.com/z4/download_fulltext.asp?pdir=scie&un=SCIE-02419 |