A dysfibrinogenemia leading to resistance to bovine thrombin
Author:
Publisher
Informa UK Limited
Subject
General Medicine
Link
http://www.tandfonline.com/doi/pdf/10.1179/2295333714Y.0000000058
Reference19 articles.
1. γ-Chain Dysfibrinogenemias: Molecular Structure-Function Relationships of Naturally Occurring Mutations in the γ Chain of Human Fibrinogen
2. Fibrinogen baltimore iv: congenital dysfibrinogenemia with a γ275 (ARG → CYS) substitution
3. Fibrinogen Hershey IV: A novel dysfibrinogen with a γV411I mutation in the integrin αIIbβ3 binding site
4. An apparently higher molecular weight gamma-chain variant in a new congenital abnormal fibrinogen Tochigi characterized by the replacement of gamma arginine-275 by cysteine
5. Identification of a dysfibrinogenemia of γR275C (Fibrinogen Fukushima)
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1. Clinical and molecular characterization of Iranian patients with congenital fibrinogen disorders;Transfusion and Apheresis Science;2021-12
2. Vorapaxar-modified polysulfone membrane with high hemocompatibility inhibits thrombosis;Materials Science and Engineering: C;2021-01
3. The amplitude of coagulation curves from thrombin time tests allows dysfibrinogenemia caused by the common mutation FGG-Arg301 to be distinguished from hypofibrinogenemia;International Journal of Laboratory Hematology;2017-03-20
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