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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Dades bibliogràfiques

Publicat a:	J Clin Invest
Autors principals:	Kramer, J, Rosen, F S, Colten, H R, Rajczy, K, Strunk, R C
Format:	Artigo
Idioma:	Inglês
Publicat:	American Society for Clinical Investigation 1993
Matèries:	Research Article
Accés en línia:	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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