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References from A novel γ-chain Tyr306Asn missense mutation causes congenital dysfibrinogenemia. Local targets link to admitted publications; unresolved targets remain external evidence.
Disorders of fibrinogen and fibrinolysis
10.1016/j.hoc.2021.07.011 · 2021 · External reference
Fibrinogen and factor XIII Subcommittee of Scientific Standardization Committee of International Society on Thrombosis and Haemostasis, recommendations for nomenclature on fibrinogen and fibrin
10.1111/j.1538-7836.2008.03242.x · 2009 · External reference
Fibrinogen function achieved through multiple covalent states
10.1038/s41467-020-19295-7 · 2020 · External reference
Clinical and molecular characterisation of 21 patients affected by quantitative fibrinogen deficiency
10.1160/th14-07-0629 · 2015 · External reference
Guideline for diagnosis and management of congenital dysfibrinogenemia
10.1016/j.cca.2024.119680 · 2024 · External reference
Laboratory and genetic investigation of mutations accounting for congenital fibrinogen disorders
10.1055/s-0036-1571340 · 2016 · External reference
Human fibrinogen: molecular and genetic aspects of congenital disorders
10.3390/ijms19061597 · 2018 · External reference
Congenital dysfibrinogenemia caused by γAla327Val mutation: structural abnormality of D region
10.1080/16078454.2021.1893977 · 2021 · External reference
Fibrinogen and fibrin
10.1016/s0065-3233(05)70008-5 · 2005 · External reference
Misdiagnosis of a patient with congenital dysfibrinogenemia: a case report and literature review
10.1002/jcla.24624 · 2022 · External reference
Congenital dysfibrinogenaemia assessed by whole blood thromboelastography
10.1111/ijlh.12827 · 2018 · External reference
Diagnosis and management of dysfibrinogenemia
2018 · External reference
Dysfibrinogenemia in a patient undergoing artificial abortion after misdiagnosis and review of the literature
10.1016/j.cca.2015.06.002 · 2015 · External reference
Natural history of patients with congenital dysfibrinogenemia
10.1182/blood-2014-06-582866 · 2015 · External reference
Recombinant fibrinogen, gamma275Arg-->Cys, exhibits formation of disulfide bond with cysteine and severely impaired D:D interactions
10.1111/j.1538-7836.2004.00600.x · 2004 · External reference
10.1016/0167-4838(83)90354-0
10.1016/0167-4838(83)90354-0 · External reference
Congenital dysfibrinogenemia in major surgery: a description of four cases and review of the literature
10.1016/j.cca.2022.01.009 · 2022 · External reference
The molecular basis of quantitative fibrinogen disorders
10.1111/j.1538-7836.2006.02094.x · 2006 · External reference
Unresolved reference
External reference
Dysfibrinogenemia: from molecular anomalies to clinical manifestations and management
10.1111/jth.12916 · 2015 · External reference
Mutational epidemiology of congenital fibrinogen disorders
10.1055/s-0038-1673685 · 2018 · External reference
10.1161/atvbaha.110.213389
10.1161/atvbaha.110.213389 · External reference
Structural basis of interfacial flexibility in fibrin oligomers
10.1016/j.str.2016.08.009 · 2016 · External reference
Fibrin formation, structure and properties
10.1007/978-3-319-49674-0_13 · 2017 · External reference
Fibrinogen and fibrin structure and functions
10.1111/j.1538-7836.2005.01365.x · 2005 · External reference
Fibrinogen Mitaka II: a hereditary dysfibrinogen with defective thrombin binding caused by an a alpha Glu-11 to Gly substitution
10.1182/blood.v82.12.3658.3658 · 1993 · External reference
Fibrinogen Nový Jicín and Praha II: cases of hereditary Aalpha 16 Arg-->Cys and Aalpha 16 Arg-->His dysfibrinogenemia
10.1016/j.thromres.2007.02.011 · 2007 · External reference
Diagnosis, clinical features and molecular assessment of the dysfibrinogenaemias
10.1111/j.1365-2516.2008.01795.x · 2008 · External reference
Two novel fibrinogen variants in the C-terminus of the bβ-chain: fibrinogen Rokycany and fibrinogen Znojmo
10.1007/s11239-010-0505-1 · 2010 · External reference
The dysfibrinogenaemias
10.1046/j.1365-2141.2001.02892.x · 2001 · External reference
Congenital dysfibrinogenemia and its laboratory investigations
2015 · External reference
Crystal structure of fragment double-D from human fibrin with two different bound ligands
10.1021/bi9804129 · 1998 · External reference
Electrospray ionization mass spectrometry identification of fibrinogen Banks Peninsula (gamma280Tyr-->Cys): a new variant with defective polymerization
10.1046/j.1365-2141.1998.00663.x · 1998 · External reference
Laboratory diagnosis of dysfibrinogenemia
10.5858/2002-126-0499-ldod · 2002 · External reference
Computational methods for prediction of human protein-phenotype associations: a review
10.1007/s43657-021-00019-w · 2021 · External reference
Women With Congenital Hypofibrinogenemia/Afibrinogenemia: from birth to death
10.1177/1076029620912819 · 2020 · External reference
Severe hereditary hypofibrinogenemia in pregnancy: a case report of a novel obstetrical management with Thromboelastometry guided fibrinogen supplementation
2025 · External reference
Familial dysfibrinogenemia and thrombophilia. Report on a study of the SSC subcommittee on fibrinogen
10.1055/s-0038-1653741 · 1995 · External reference
Dysfibrinogenemia during pregnancy treated successfully with fibrinogen
10.1034/j.1600-0412.2003.00211.x · 2003 · External reference
