[Analysis of phenotype and genotype in a Chinese pedigree with inherited prothrombin deficiency resulted from a homozygous mutation Tyr510Asp]

Zhonghua Xue Ye Xue Za Zhi. 2012 Jul;33(7):587-9.
[Article in Chinese]
No abstract available

Publication types

  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Adolescent
  • Adult
  • Amino Acid Sequence
  • Genotype
  • Homozygote
  • Humans
  • Hypoprothrombinemias / etiology*
  • Hypoprothrombinemias / genetics*
  • Male
  • Middle Aged
  • Molecular Sequence Data
  • Mutation*
  • Pedigree
  • Phenotype
  • Young Adult