A Nonsense Mutation in FGA g.3807C→T (p.R159X) Causes Afibrinogenaemia in the Homozygous Form
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Published:2009
Issue:4
Volume:121
Page:216-217
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ISSN:0001-5792
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Container-title:Acta Haematologica
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language:en
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Short-container-title:Acta Haematol
Author:
Marchi Cappelletti R.,Tersek Y.,Ruiz-Sáez A.,Meyer M.
Subject
Hematology,General Medicine
Cited by
1 articles.
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