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A molecular model of a point mutation (Val297Met) in the serine protease domain of protein C

Song KS, Park YS, Choi JR, Kim HK, Park Q

  • KMID: 755027
  • Exp Mol Med.
  • 1999 Mar;31(1):47-51.
A heterozygous GTG to ATG (Val297Met) mutation was detected in a patient with inherited protein C deficiency and deep vein thrombosis. Cosegregation of the mutation with protein C deficiency was observed through...
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