Mapping the Bst Mutation on Mouse Chromosome 16: A Model for Human Optic Atrophy

Mamm Genome. 1995 Aug;6(8):546-8. doi: 10.1007/BF00356174.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Chromosome Mapping*
  • Crosses, Genetic
  • Disease Models, Animal
  • Female
  • Heterozygote
  • Humans
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mutation*
  • Optic Atrophies, Hereditary / genetics*