Scott syndrome, characterized by impaired transmembrane migration of procoagulant phosphatidylserine and hemorrhagic complications, is an inherited disorder (Q71017541)
scientific article published on 01 February 1996
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(P31) (Q13442814)
(P304) 1409-1415
(P407) (Q1860)
(P433) 4
(P478) 87
(P577) Thursday, February 1, 1996
(P921) (Q7437571)
(P1104) 7
(P1433) (Q885070)
(P1476) "Scott syndrome, characterized by impaired transmembrane migration of procoagulant phosphatidylserine and hemorrhagic complications, is an inherited disorder" (language: en)
(P2093) Toti F
Satta N
Fressinaud E
Meyer D
Freyssinet JM
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description scientific article published on 01 February 1996

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