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A Nonsense Mutation in FGA g.3807C→T (p.R159X) Causes Afibrinogenaemia in the Homozygous Form

Acta Haematol (2009) 121 (4): 216–217.
This article has been cited by the following articles in journals that are participating in CrossRef Cited-by Linking.
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Research and Practice in Thrombosis and Haemostasis (2021) 5 (6): e12568.
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