2176insC: a novel mutation in exon 13 of the cystic fibrosis gene

Hum Hered. 1996 May-Jun;46(3):166-7. doi: 10.1159/000154346.
No abstract available

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Child
  • Cystic Fibrosis / genetics*
  • Exons*
  • Humans
  • Male
  • Mutagenesis, Insertional*