Homozygous Rare PARN Missense Mutation in Familial Pulmonary Fibrosis

Antzeko izenburuak

• Rare Genetic Variants in PARN Are Associated with Pulmonary Fibrosis in Families
  nork: Kropski, Jonathan A., et al.
  Argitaratua: (2017)
• Familial Pulmonary Fibrosis and Hermansky-Pudlak Syndrome Rare Missense Mutations in Context
  nork: Stearman, Robert S., et al.
  Argitaratua: (2019)
• Exome Sequencing Links Mutations in PARN and RTEL1 with Familial Pulmonary Fibrosis and Telomere Shortening
  nork: Stuart, Bridget D., et al.
  Argitaratua: (2015)
• A rare homozygous missense mutation of COL7A1 in a Vietnamese family
  nork: Nguyen Thuy Duong, et al.
  Argitaratua: (2022-05-01)
• Telomere Shortening in Familial and Sporadic Pulmonary Fibrosis
  nork: Cronkhite, Jennifer T., et al.
  Argitaratua: (2008)