Afibrinogenemia resulting from homozygous nonsense mutation in A alpha chain gene associated with multiple thrombotic episodes.

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Published in Blood Coagul Fibrinolysis on April 01, 2008

Authors

Ismail Simsek1, Philippe de Mazancourt, Marie-Hèléne Horellou, Hakan Erdem, Salih Pay, Ayhan Dinc, Meyer Michel Samama

Author Affiliations

1: Gulhane Military School of Medicine, Division of Rheumatology, Ankara, Turkey. isimsek@gata.edu.tr

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