Scott syndrome, characterized by impaired transmembrane migration of procoagulant phosphatidylserine and hemorrhagic complications, is an inherited disorder.

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Published in Blood on February 15, 1996

Authors

F Toti1, N Satta, E Fressinaud, D Meyer, J M Freyssinet

Author Affiliations

1: Institut d'Hématolgoie et Immunologie, Faculté de Médecine, Université Louis Pasteur, Strasbourg, France.

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