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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...

詳細記述

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書誌詳細
主要な著者: Kramer, J, Rosen, F S, Colten, H R, Rajczy, K, Strunk, R C
フォーマット: Artigo
言語:Inglês
出版事項: 1993
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC288087/
https://ncbi.nlm.nih.gov/pubmed/8450054
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