Associated Papers
F8 IVS9+5G>A mutation causes moderate haemophilia A.
Li D et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia, 2019
PROS1 IVS10+5G>A mutation causes hereditary protein S deficiency in a Chinese patient with pulmonary embolism and venous thromboembolism.
Wang X et al.
Thrombosis Research, 2019
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