Restriction fragment length polymorphism of the C1 inhibitor gene in hereditary angioneurotic edema.
Hereditary angioneurotic edema (HANE) results from the deficiency of the inhibitor of the first component of human complement (C1-INH). It is inherited as an autosomal dominant trait. Heterogeneity of this defect has been shown at the protein and mRNA level. Southern blot analysis of genomic DNA was...
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| Pubblicato in: | J Clin Invest |
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| Autori principali: | , , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
American Society for Clinical Investigation
1987
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC442434/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/2890659/ https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI113252 |
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