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Mutation of the translation initiation codon in FGA causes congenital afibrinogenemia.
Tirefort Y, Alson OR, de Moerloose P, Neerman-Arbez M.
Blood Coagul Fibrinolysis. 2012 Sep;23(6):556-8. doi: 10.1097/MBC.0b013e328355a76e.
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