Transinhibition of C1 inhibitor synthesis in type I hereditary angioneurotic edema.

To ascertain the mechanism for decreased synthesis of C1 inhibitor (C1 INH) in certain patients with the autosomal dominant disorder hereditary angioneurotic edema, we studied expression of C1 INH in fibroblasts in which the mutant and wild type mRNA and protein could be distinguished because of del...

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Veröffentlicht in:	J Clin Invest
Hauptverfasser:	Kramer, J, Rosen, F S, Colten, H R, Rajczy, K, Strunk, R C
Format:	Artigo
Sprache:	Inglês
Veröffentlicht:	American Society for Clinical Investigation 1993
Schlagworte:	Research Article
Online-Zugang:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC288087/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/8450054/ https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI116290
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