Stedman's > antithrombin III

antithrombin III

a plasma α₂-globulin process that inhibits thrombin and has anticoagulant activities. Deficiency [MIM*107300] is commonly inherited as an autosomal dominant trait, caused by mutation in antithrombin III gene (AT₃) or chromosome 1q; this is one of the few known mendelizing disorders from which thrombotic disease occurs.

 

 

 

 

 

 

 

 

 

 

 

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