Confirmation of inherited protein S deficiency by PROS1 mutational screening: Identification of three novel PROS1 mutations and haplotype analysis of p.Q279X recurrence

Thromb Haemost. 2008 Oct;100(4):721-4.
No abstract available

Publication types

  • Letter

MeSH terms

  • Amino Acid Sequence
  • DNA Mutational Analysis
  • Female
  • Genetic Testing*
  • Haplotypes
  • Humans
  • Male
  • Molecular Sequence Data
  • Protein S / chemistry
  • Protein S / genetics*
  • Protein S Deficiency / diagnosis*
  • Protein S Deficiency / genetics*
  • Structure-Activity Relationship

Substances

  • Protein S