Homozygous Rare PARN Missense Mutation in Familial Pulmonary Fibrosis

Am J Respir Crit Care Med. 2019 Mar 15;199(6):797-799. doi: 10.1164/rccm.201809-1632LE.
No abstract available

Publication types

  • Letter
  • Research Support, N.I.H., Extramural

MeSH terms

  • Female
  • Genetic Predisposition to Disease*
  • Homozygote*
  • Humans
  • Male
  • Middle Aged
  • Mutation, Missense*
  • Pulmonary Fibrosis / diagnosis*
  • Pulmonary Fibrosis / genetics*
  • Texas