Mutations in the endothelin-receptor B gene in Hirschsprung disease in Sweden

Clin Genet. 1999 Mar;55(3):215-7. doi: 10.1034/j.1399-0004.1999.550312.x.
No abstract available

Publication types

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

MeSH terms

  • Amino Acid Substitution
  • Family Health
  • Female
  • Hirschsprung Disease / genetics*
  • Humans
  • Male
  • Mutation
  • Pedigree
  • Point Mutation
  • Receptor, Endothelin B
  • Receptors, Endothelin / genetics*
  • Sweden

Substances

  • Receptor, Endothelin B
  • Receptors, Endothelin