𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Mutation screening of C1 inhibitor gene in 108 unrelated families with hereditary angioedema: Functional and structural correlates

✍ Scribed by Emanuela Pappalardo; Sonia Caccia; Chiara Suffritti; Attila Tordai; Lorenza Chiara Zingale; Marco Cicardi


Book ID
116756860
Publisher
Elsevier Science
Year
2008
Tongue
English
Weight
267 KB
Volume
45
Category
Article
ISSN
0161-5890

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


Mutation screening of the C1 inhibitor g
✍ Lajos KalmΓ‘r; AndrΓ‘s Bors; Henriette Farkas; Szilvia Vas; Barbara Fandl; Lilian πŸ“‚ Article πŸ“… 2003 πŸ› John Wiley and Sons 🌐 English βš– 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