Mutation screening of the C1 inhibitor g
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Lajos KalmΓ‘r; AndrΓ‘s Bors; Henriette Farkas; Szilvia Vas; Barbara Fandl; Lilian
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Article
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2003
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John Wiley and Sons
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English
β 67 KB
Hereditary angioneurotic edema (HAE) is an autosomal dominant disorder characterized by episodic local subcutaneous and submucosal edema caused by the deficiency of activated C1 esterase inhibitor protein (C1-INH, type I (C1NH): reduced serum antigen level, type II: reduced activity and normal serum