Missense mutations in the coagulation factor XII (Hageman factor) gene in hereditary angioedema with normal C1 inhibitor
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry,Biophysics
Reference14 articles.
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3. Detection of C1 inhibitor mutations in patients with hereditary angioedema;Zuraw;J. Allergy Clin. Immunol.,2000
4. A review of the reported defects in the human C1 esterase inhibitor gene producing hereditary angioedema including four new mutations;Bowen;Clin. Immunol.,2001
5. Hereditary angioedema with normal C1-inhibitor in women;Bork;Lancet,2000
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