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Novel factor VII gene mutations in six families with hereditary coagulation factor VII deficiency.

Xiaoyu ZhangShuwen WangShaoqiu LengQi FengYanqi ZhangShuqian XuLei ZhangXinsheng ZhangYunhai FangJun PengZi Sheng
Published in: Journal of clinical laboratory analysis (2021)
We have identified novel genetic mutations and performed pedigree analysis that shed light on the pathogenesis of hereditary human coagulation FVII deficiency and may contribute to the development of treatments for this disease.
Keyphrases
  • endothelial cells
  • replacement therapy
  • induced pluripotent stem cells
  • genome wide
  • pluripotent stem cells
  • gene expression
  • copy number