Human Fibrinogen: Molecular and Genetic Aspects of Congenital Disorders
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Title
Human Fibrinogen: Molecular and Genetic Aspects of Congenital Disorders
Authors
Keywords
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Journal
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES
Volume 19, Issue 6, Pages 1597
Publisher
MDPI AG
Online
2018-05-30
DOI
10.3390/ijms19061597
References
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Related references
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- A novel fibrinogen gamma chain mutation (c.1096C>G; p.His340Asp), fibrinogen Ankara, causing hypofibrinogenaemia and hepatic storage
- (2017) Francesco Callea et al. PATHOLOGY
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- Fibrinogen Martin: A Novel Mutation in FGB (Gln180Stop) Causing Congenital Afibrinogenemia
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- (2016) C. Berens et al. THROMBOSIS AND HAEMOSTASIS
- Thromboembolism in patients with congenital afibrinogenaemia
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- (2014) A. Casini et al. BLOOD
- Molecular Pathology of Rare Bleeding Disorders (RBDs) in India: A Systematic Review
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- (2010) Benoît Polack et al. TRANSFUSION
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