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Thromb Haemost 2007; 98(03): 689-691
DOI: 10.1160/TH07-01-0075
DOI: 10.1160/TH07-01-0075
Letters to the Editor
Clinical and biological features of 3 cases of hypofibrinogenemia associated with three different mutations(γAla341Thr, Bβ Tyr326Cys and Aα Asp496Asn)
Authors
Further Information
Publication History
Received
31 January 2007
Accepted after resubmission
13 June 2007
Publication Date:
28 November 2017 (online)
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References
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- 3 Sheen CR, Brennan SO, Jabado N. et al. Fibrinogen Montreal: a novel missense mutation (Aα D496N) associated with hypofibrinogenaemia. Thromb Haemost 2006; 96: 231-232.
- 4 Sheen CR, Low J, Joseph J. et al. Fibrinogen Darlinghurst: hypofibrinogenaemia caused by a W253G mutation in the gamma chain in a patient with both bleeding and thrombotic complications. Thromb Haemost 2006; 96: 685-687.
- 5 Vu D, de Moerloose P, Batorova A. et al. Hypofibrinogenaemia caused by a novel FGG missense mutation (W253C) in the gamma chain globular domain impairing fibrinogen secretion. J Med Genet 2005; 42: e57.
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- 9 Dear A, Dempfle CE, Brennan SO. et al. Fibrinogen Mannheim II: a novel gamma307 His→Tyr substitution in the gammaD domain causes hypofibrinogenemia. J Thromb Haemost 2004; 2: 2194-2199.
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