Novel fibrinogen Aα chain mutation associated with afibrinogenaemia
Author:
Publisher
Elsevier BV
Subject
Pathology and Forensic Medicine
Reference11 articles.
1. Molecular mechanisms of hypo- and afibrinogenemia;Brennan;Ann NY Acad Sci,2001
2. The molecular mechanisms of congenital hypofibrinogenaemia;Maghzal;Cell Mol Life Sci,2004
3. Fibrinogen Mannheim II: a novel y307 His→Tyr substitution in the yD domain causes hypofibrinogenaemia;Dear;J Thromb Haemost,2004
4. Congenital afibrinogenemia: mutations leading to premature termination codons in fibrinogen Aa-chain gene are not associated with the decay of the mutant mRNAs;Asselta;Blood,2001
5. Prophylactic cryoprecipitate in congenital afibrinogenemia;Rodriguez;Clin Pediatr,1988
Cited by 1 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. A Nonsense Mutation in FGA g.3807C→T (p.R159X) Causes Afibrinogenaemia in the Homozygous Form;Acta Haematologica;2009
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