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A Case of Type 2 Hereditary Angioedema With SERPING1 Mutation
Hereditary angioedema is a disease of congenital deficiency or functional defect in the C1 esterase inhibitor (C1-INH) consequent to mutation in the SERPING1 gene, which encodes C1-INH. This disease manifests as recurrent, non-pitting, non-pruritic subcutaneous, or submucosal edema as well as an ery...
Tallennettuna:
| Julkaisussa: | Allergy Asthma Immunol Res |
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| Päätekijät: | , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
The Korean Academy of Asthma, Allergy and Clinical Immunology; The Korean Academy of Pediatric Allergy and Respiratory Disease
2017
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5102842/ https://ncbi.nlm.nih.gov/pubmed/27826968 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4168/aair.2017.9.1.96 |
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