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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...
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| Publicado en: | Genes (Basel) |
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| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
MDPI
2021
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| Assuntos: | |
| Acceso en liña: | 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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