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doi: 10.1166/jnn.2020.17486, 105

This process is most clearly understood for factor II, also called preprothrombin

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Introduction -thalassemia is an autosomal recessive genetic disorder characterized by impaired erythropoiesis due to point mutations in the splice site or promoter sites of the -globin genes on chromosome 11

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Diabetes Care 36 , 10471055 (2013)