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The Global Registry for Hereditary Angioedema due to C1-Inhibitor Deficiency
Hereditary angioedema (HAE) is a rare condition, mostly due to genetic deficiency of complement C1 inhibitor (C1-INH). The rarity of HAE impedes extensive data collection and assessment of the impact of certain factors known to affect the course of this disabling and life-threatening disease. Establ...
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| 發表在: | Clin Rev Allergy Immunol |
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| Main Authors: | , , , , , , , , , , , |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
Springer US
2021
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| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8282542/ https://ncbi.nlm.nih.gov/pubmed/33791951 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s12016-021-08855-4 |
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