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Inherited C1 inhibitor deficiency.

Complement and inflammation, 1989
The paper reports our experience of a 15-year follow-up of 179 patients with hereditary angioedema (HAE). The disease is transmitted as an autosomal dominant trait and two variants have been described: type I characterized by functional and antigenic C1-inhibitor (C1-INH) deficiency and type II with normal or upper normal C1-INH antigenic levels but no
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C1 INHIBITOR IN MALIGNANT DISEASES

The Lancet, 1976
P J, Lachmann, J, Wragge-Morley
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