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Novel IRF6 mutations in Chinese Han families with Van der Woude syndrome.

Yanqin YuYatao WanChuanqi QinHaitang YueZhuan BianMiao He
Published in: Molecular genetics & genomic medicine (2020)
Our study has advanced the understanding of the genetic architecture of VWS and provides the basis for genetic counseling, antenatal diagnosis, and gene therapy of high risk groups.
Keyphrases
  • gene therapy
  • genome wide
  • pregnant women
  • copy number
  • dendritic cells
  • preterm birth
  • case report
  • gene expression