Antithrombin Deficiency Is Associated with a Novel Homozygous Detrimental Mutation in SERPINC1 Gene in a Saudi Female
Sign Up to like & getrecommendations! Published in 2023 at "Case Reports in Medicine"
DOI: 10.1155/2023/8872346
Abstract: Antithrombin (AT) deficiency is a blood disorder associated with an increased tendency to form thrombosis. Hereditary AT deficiency is frequently caused by mutations in SERPINC1 gene. It is usually inherited as an autosomal dominant with… read more here.
Keywords: serpinc1 gene; antithrombin deficiency; mutation; gene ... See more keywords
Utility of the SERPINC1 Gene Test in Ischemic Stroke Patients With Antithrombin Deficiency
Sign Up to like & getrecommendations! Published in 2022 at "Frontiers in Neurology"
DOI: 10.3389/fneur.2022.841934
Abstract: Objective Antithrombin (AT) plays a critical role in the coagulation system, and its deficiency induces hypercoagulability. AT deficiency is caused not only by inherited variants in the SERPINC1 gene but also by acquired conditions. Therefore,… read more here.
Keywords: serpinc1 gene; gene test; gene; deficiency ... See more keywords