Associated Papers
A thrombophilia family with protein S deficiency due to protein translation disorders caused by a Leu607Ser heterozygous mutation in PROS1.
Zhang YP et al.
Thrombosis Journal, 2021
Two Novel Variants in the Protein S Gene PROS1 Are Associated with Protein S Deficiency and Thrombophilia.
Juhl D et al.
Acta Haematologica, 2021
[Recurrent deep vein thrombosis caused by heterozygous missense mutation of the protein S gene: genetic analysis of a case].
Ye X et al.
Nan Fang Yi Ke Da Xue Xue Bao = Journal of Southern Medical University, 2011
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