TY  - JOUR
AU  - López-Lera, Alberto
AU  - Sanchez-Cabo, Fatima
AU  - Garrido, Sofía
AU  - Dopazo, Ana
AU  - López-Trascasa, Margarita
PY  - 2013
DO  - 10.1186/1750-1172-8-77
SN  - 1750-1172
UR  - http://hdl.handle.net/20.500.12105/7571
AB  - BACKGROUND: Hereditary Angioedema due to C1-Inhibitor deficiency (HAE types I and II) is a monogenic disease characterized by sudden, self-limited episodes of cutaneous and mucosal swelling due to local deregulation of vascular permeability. Despite...
LA  - eng
PB  - BioMed Central (BMC)
KW  - Complement C1 Inhibitor Protein
KW  - Family
KW  - Female
KW  - Gene Expression Regulation
TI  - Disease-modifying factors in hereditary angioedema: an RNA expression-based screening
TY  - journal article
ER  -