Associated Papers
Distinctive regional-specific PROS1 mutation spectrum in Southern China.
Chan NCN et al.
Journal of Thrombosis and Thrombolysis, 2018
Gene analysis of six cases of congenital protein S deficiency and functional analysis of protein S mutations (A139V, C449F, R451Q, C475F, A525V and D599TfsTer13).
Taniguchi F et al.
Thrombosis Research, 2017
PROS1 analysis in 87 pedigrees with hereditary protein S deficiency demonstrates striking genotype-phenotype associations.
Ten Kate MK et al.
Human Mutation, 2008
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