Title : A heparin cofactor II mutation (HCII Rimini) combined with factor V Leiden or type I protein C deficiency in two unrelated thrombophilic subjects.

Pub. Date : 1996 Oct

PMID : 8902986






1 Functional Relationships(s)
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1 The heparin cofactor II gene alteration was associated with, in one patient, the factor V Leiden mutation and, in the other, type I protein C deficiency. Heparin coagulation factor V Homo sapiens