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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)
Weitere Informationen
Publikationsverlauf
Received
31. Januar 2007
Accepted after resubmission
13. Juni 2007
Publikationsdatum:
28. November 2017 (online)
![](https://www.thieme-connect.de/media/10.1055-s-00035024/200703/lookinside/thumbnails/10-1160-th07-01-0075-1.jpg)
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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.
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