Molecular basis for the deficiency of complement 1 inhibitor in type I hereditary angioneurotic edema.
Hereditary angioneurotic edema (HANE) results from deficiency of complement 1 inhibitor (C1 INH). In type I HANE, C1 INH is present in serum at levels 5-30% of normals. Using cultured monocytes and biosynthetic labeling of proteins, C1 INH was detected in supernatants of cells from HANE patients at...
में बचाया:
| में प्रकाशित: | J Clin Invest |
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| मुख्य लेखकों: | , , , |
| स्वरूप: | Artigo |
| भाषा: | Inglês |
| प्रकाशित: |
American Society for Clinical Investigation
1987
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| विषय: | |
| ऑनलाइन पहुंच: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC424179/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/3818946/ https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI112873 |
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