Disruption of the C7orf2/Lmbr1 genic region is associated with preaxial polydactyly in humans and mice

J Bone Miner Metab. 2003;21(1):1-4. doi: 10.1007/s007740300000.
No abstract available

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Chromosomes, Human, Pair 5
  • Chromosomes, Human, Pair 7
  • Humans
  • Membrane Proteins / genetics*
  • Mice
  • Mutation*
  • Open Reading Frames
  • Polydactyly / genetics*
  • Translocation, Genetic

Substances

  • LMBR1 protein, human
  • Lmbr1 protein, mouse
  • Membrane Proteins

Associated data

  • OMIM/190605
  • OMIM/200500