Associated Papers
Establishment and genetic characterization of zebrafish RW line.
Sadamitsu K et al.
Scientific Reports, 2025
40281206 (PubMed )
Supplement: 41598_2025_98674_MOESM2_ESM.xlsx › Table_S10__IND_
Mutations Accounting for Congenital Fibrinogen Disorders: An Update.
Richard M et al.
Seminars in Thrombosis and Hemostasis, 2022
Clinical and molecular characterization of Iranian patients with congenital fibrinogen disorders.
Mohsenian S et al.
Transfusion and Apheresis Science : Official Journal of the World Apheresis Association : Official Journal of the European Society for Haemapheresis, 2021
Pseudohomozygous dysfibrinogenemia.
Peck RC et al.
Research and Practice in Thrombosis and Haemostasis, 2021
Molecular and clinical profile of congenital fibrinogen disorders in Iran, identification of two novel mutations.
Tavasoli B et al.
International Journal of Laboratory Hematology, 2020
Identification and characterization of novel mutations implicated in congenital fibrinogen disorders.
Smith N et al.
Research and Practice in Thrombosis and Haemostasis, 2018
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