High frequency of the R117H cystic fibrosis mutation in patients with congenital absence of the vas deferens

N Engl J Med. 1993 Feb 11;328(6):446-7. doi: 10.1056/NEJM199302113280619.
No abstract available

Publication types

  • Letter

MeSH terms

  • Adult
  • Cystic Fibrosis / genetics*
  • Exons
  • Humans
  • Male
  • Mutation
  • Vas Deferens / abnormalities*