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Clinical and biological features of 3 cases of hypofibrinogenemia associated with three different mutations (gamma Ala341Thr, Bbeta Tyr326Cys and Aalpha Asp496Asn).

Thrombosis and haemostasis - 1 Sept 2007

Hanss Michel, Chevreaud Caroline, French Patrick, Négrier Claude, de Mazancourt Philippe

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Share to Afibrinogenemia
Share to Blood Coagulation
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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PMID: 17849064

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026.

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