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Journal of Clinical Lipidology, ISSN 1933-2874, 2016, Volume 10, Issue 4, pp. 816 - 823
Journal Article
Journal Article
Thrombosis Research, ISSN 0049-3848, 10/2017, Volume 158, pp. 134 - 137
We report four children from different families with homozygous antithrombin (AT) deficiency type II affecting the heparin binding site (p.Leu131Phe mutation).... 
LMWH | vitamin K antagonists | antithrombin | HBS | low-molecular-weight heparin | heparin binding site | VKA | ENOXAPARIN | METAANALYSIS | THERAPY | HUMAN COAGULATION SYSTEM | THROMBOPHILIA | MUTATION | PERIPHERAL VASCULAR DISEASE | THROMBOEMBOLISM | INFANT | HEMATOLOGY | VARIANT | CHILDREN | Infants (Newborn) | Medical colleges | Genetic disorders | Heparin | Thromboembolism
Journal Article
Journal Article
Journal Article