Frequency of the p.Thr241Asn mutation in Chinese patients with congenital factor VII deficiency

Thromb Res. 2024 Mar:235:122-124. doi: 10.1016/j.thromres.2024.02.006. Epub 2024 Feb 6.
No abstract available

Keywords: F7; Factor VII deficiency; Genotype-phenotype; Hemorrhage; Mutation.

Publication types

  • Letter

MeSH terms

  • China
  • Factor VII Deficiency* / genetics
  • Humans

Substances

  • ATP2C1 protein, human