Familial spontaneous pneumothorax and FBN1 mutations

Am J Respir Crit Care Med. 2004 Jun 1;169(11):1260-2. doi: 10.1164/ajrccm.169.11.967.
No abstract available

Publication types

  • Letter

MeSH terms

  • Alleles
  • Chromosomes, Human, Pair 15 / genetics
  • Family Health
  • Fibrillin-1
  • Fibrillins
  • Genetic Predisposition to Disease / genetics
  • Genome, Human
  • Genotype
  • Humans
  • Marfan Syndrome / genetics
  • Microfilament Proteins / genetics*
  • Pedigree
  • Pneumothorax / genetics*
  • Point Mutation / genetics

Substances

  • FBN1 protein, human
  • Fibrillin-1
  • Fibrillins
  • Microfilament Proteins