TY  - JOUR 
AU  - Blanch, Alvaro
AU  - Roche, Olga
AU  - Urrutia, Ignacio
AU  - Gamboa, Pedro
AU  - Fontán, Gumersindo
AU  - López-Trascasa, Margarita
PY  - 2006
SN  - 0091-6749
UR  - http://hdl.handle.net/20.500.12020/1140
AB  - Background: C1 Inhibitor (C1-Inh) deficiency causes angioedema and can be hereditary (HAE), caused by mutations in the C1-Inh gene (C1NH), or acquired (AAE). Patients with HAE show a complement profile different from that of patients with AAE with...
LA  - en
PB  - Elsevier
TI  - First case of homozygous C1 inhibitor deficiency
DO  - https://doi.org/10.1016/j.jaci.2006.07.035
T2  - Journal of Allergy and Clinical Immunology
M2  - 1330
KW  - Hereditary Angioedema
KW  - C1 Inhibitor
KW  - Classical Complement Activation Pathway
KW  - Homozygous C1NH Mutation
KW  - Serine Protease Inhibitor
VL  - 118
ER  -