The clinical complexity of PKHD1 gene: from neonatal lethality to casual diagnosis in late pediatric stages

An Pediatr (Engl Ed). 2024 Jun;100(6):467-471. doi: 10.1016/j.anpede.2024.04.014. Epub 2024 Jun 4.
No abstract available

Publication types

  • Letter
  • Case Reports

MeSH terms

  • Female
  • Humans
  • Infant
  • Infant, Newborn
  • Male
  • Mutation
  • Receptors, Cell Surface* / genetics

Substances

  • PKHD1 protein, human
  • Receptors, Cell Surface