TY  - GEN
AU  - Loreth,R M
AU  - Meyer,M
AU  - Albert,F W
TI  - Fibrinogen kaiserslautern III: a new case of congenital dysfibrinogenemia with aalpha 16 arg-->cys substitution
SN  - 0301-0147
PY  - 2001///0906
KW  - Blood Coagulation Disorders
KW  - congenital
KW  - Blood Coagulation Tests
KW  - Family Health
KW  - Fibrinogens, Abnormal
KW  - genetics
KW  - Fibrinopeptide A
KW  - metabolism
KW  - Fibrinopeptide B
KW  - Hemorrhage
KW  - etiology
KW  - Humans
KW  - Male
KW  - Middle Aged
KW  - Point Mutation
KW  - Sequence Analysis, DNA
KW  - Thrombin
KW  - pharmacology
N1  - Publication Type: Case Reports; Journal Article
UR  - https://doi.org/10.1159/000048039
ER  -