Interstitial lung disease in a child heterozygous for the 1549C-->GAA (121ins2) mutation of surfactant protein B

Eur Respir J. 2011 Oct;38(4):985-7. doi: 10.1183/09031936.00155310.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Heterozygote
  • Humans
  • Infant
  • Lung Diseases, Interstitial / diagnostic imaging
  • Lung Diseases, Interstitial / genetics*
  • Male
  • Point Mutation / genetics*
  • Pulmonary Surfactant-Associated Protein B / genetics*
  • Radiography

Substances

  • Pulmonary Surfactant-Associated Protein B