A novel mutation in exon 2 of FGB caused by c.221G>T † substitution, predicting the replacement of the native Arginine at position 74 with a Leucine (p.Arg74Leu † ) in a proband from a Kurdish family with dysfibrinogenaemia and familial venous and arterial thrombosis-Reference-Cited by-同舟云学术

A novel mutation in exon 2 of FGB caused by c.221G>T † substitution, predicting the replacement of the native Arginine at position 74 with a Leucine (p.Arg74Leu † ) in a proband from a Kurdish family with dysfibrinogenaemia and familial venous and arterial thrombosis

Published:2016-11-03 Issue:2 Volume:43 Page:263-270
ISSN:0929-5305
Container-title:Journal of Thrombosis and Thrombolysis
language:en
Short-container-title:J Thromb Thrombolysis

Author:

Shlebak Abdul A.,Katsarou Alexia D.,Adams George,Fernando Fiona

Publisher

Springer Science and Business Media LLC

Subject

Cardiology and Cardiovascular Medicine,Hematology

Link

http://link.springer.com/content/pdf/10.1007/s11239-016-1439-z.pdf

Reference41 articles.

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2. de Moerloose P, Casini A, Neerman-Arbez M (2013) Congenital fibrinogen disorders: an update. Semin Thromb Hemost 39: 585–595

3. McDonagh J (2001) Dysfibrinogenemia and other disorders of fibrinogen structure or function. In: Colman R, Hirsh J, Marder V, Clowes A, George J, (editors). Hemostasis and thrombosis. 4th edn. Lippincott Williams & Wilkins, Philadelphia, pp 855–892

4. Ebert R (1994) Index of variant human fibrinogens. CRC Press, Boca Raton

5. Haverkate F, Samama M (1995) Familial dysfibrinogenemia and thrombophilia: report on a study of the SCC Subcommittee on Fibrinogen. Thromb Haemost 73:151–161

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