TY  - GEN
AU  - Kluft,C
AU  - Nieuwenhuis,H K
AU  - Vellenga,E
TI  - Congenital deficiencies in alpha 2-antiplasmin
SN  - 0390-5748
PY  - 1985///0308
KW  - Binding Sites
KW  - Blood Coagulation Disorders
KW  - congenital
KW  - Fibrin
KW  - metabolism
KW  - Fibrinolysin
KW  - Fibrinolysis
KW  - Genetic Carrier Screening
KW  - Homozygote
KW  - Humans
KW  - Lysine
KW  - Methods
KW  - Plasminogen
KW  - alpha-2-Antiplasmin
KW  - analysis
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Review
UR  - https://doi.org/10.1007/BF02904878
ER  -