TY  - GEN
AU  - Denninger,M H
AU  - Finlayson,J S
AU  - Reamer,L A
AU  - Parquet-Gernez,A
AU  - Goudemand,M
AU  - Menache,D
TI  - Congenital dysfibrinogenemia: fibrinogen Lille
SN  - 0049-3848
PY  - 1979///0428
KW  - Ancrod
KW  - metabolism
KW  - Batroxobin
KW  - Blood Coagulation Disorders
KW  - congenital
KW  - Blood Coagulation Tests
KW  - Blood Protein Electrophoresis
KW  - Child
KW  - Endopeptidases
KW  - Female
KW  - Fibrin Fibrinogen Degradation Products
KW  - analysis
KW  - Fibrinogen
KW  - Fibrinopeptide A
KW  - Humans
KW  - Immunoelectrophoresis
KW  - Structure-Activity Relationship
KW  - Thrombin
N1  - Publication Type: Case Reports; Journal Article
UR  - https://doi.org/10.1016/0049-3848(78)90131-7
ER  -