Molecular basis for the deficiency of complement 1 inhibitor in type I hereditary angioneurotic edema.
Cicardi, M
Molecular basis for the deficiency of complement 1 inhibitor in type I hereditary angioneurotic edema. [electronic resource] - The Journal of clinical investigation Mar 1987 - 698-702 p. digital
Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
0021-9738
10.1172/JCI112873 doi
Angioedema--blood
Cells, Cultured
Complement C1 Inactivator Proteins--blood
DNA--genetics
Humans
Monocytes--metabolism
Nucleic Acid Hybridization
RNA, Messenger--metabolism
Molecular basis for the deficiency of complement 1 inhibitor in type I hereditary angioneurotic edema. [electronic resource] - The Journal of clinical investigation Mar 1987 - 698-702 p. digital
Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
0021-9738
10.1172/JCI112873 doi
Angioedema--blood
Cells, Cultured
Complement C1 Inactivator Proteins--blood
DNA--genetics
Humans
Monocytes--metabolism
Nucleic Acid Hybridization
RNA, Messenger--metabolism