DOI:
10.1055/s-00000077
Seminars in Thrombosis and Hemostasis
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References
Takezawa Y, Terasawa F, Matsuda K , et al.
Molecular analysis of afibrinogenemic mutations caused by a homozygous FGA1238 bp deletion, and a compound heterozygous FGA1238 bp deletion and novel FGA c.54+3A>C substitution.
Int J Hematol 2012;
96 (1) 39-46
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