Associated Papers
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
Inherited protein S deficiency due to a novel nonsense mutation in the PROS1 gene in the patient with recurrent vascular access thrombosis: A case report.
Cho EJ et al.
Kidney Research and Clinical Practice, 2012
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