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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 SERPING1 gene encoding C1-inhibitor (C1-INH-HA...
Salvato in:
| Pubblicato in: | Genes (Basel) |
|---|---|
| Autori principali: | , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
MDPI
2021
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7998782/ https://ncbi.nlm.nih.gov/pubmed/33799813 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/genes12030402 |
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