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...
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| Formatua: | Artigo |
| Hizkuntza: | Inglês |
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KARE Publishing
2019-12-01
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| Saila: | Southern Clinics of Istanbul Eurasia |
| Gaiak: | |
| Sarrera elektronikoa: | https://jag.journalagent.com/z4/download_fulltext.asp?pdir=scie&un=SCIE-02419 |
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