Rapid genetic diagnosis of neonatal persistent pulmonary hypertension with a novel FOXF1 mutation

Pediatr Neonatol. 2023 Jul;64(4):484-486. doi: 10.1016/j.pedneo.2022.12.010. Epub 2023 Jan 25.
No abstract available

Publication types

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

MeSH terms

  • Forkhead Transcription Factors / genetics
  • Humans
  • Hypertension, Pulmonary* / diagnosis
  • Hypertension, Pulmonary* / genetics
  • Infant, Newborn
  • Lung
  • Mutation
  • Persistent Fetal Circulation Syndrome* / diagnosis
  • Persistent Fetal Circulation Syndrome* / genetics

Substances

  • Forkhead Transcription Factors
  • FOXF1 protein, human