Associated Papers
Phenotypic and genetic analysis of dysprothrombinemia due to a novel homozygous mutation.
Su K et al.
Hematology (amsterdam, Netherlands), 2017
A novel congenital dysprothrombinemia leading to defective prothrombin maturation.
Bafunno V et al.
Thrombosis Research, 2014
Molecular genetics of hereditary prothrombin deficiency in Indian patients: identification of a novel Ala362 --> Thr (Prothrombin Vellore 1) mutation.
Jayandharan G et al.
Journal of Thrombosis and Haemostasis : Jth, 2005
Identification and three-dimensional structural analysis of nine novel mutations in patients with prothrombin deficiency.
Akhavan S et al.
Thrombosis and Haemostasis, 2000
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