Cellular Retinol Binding Protein 1 (RBP1): a frequent polymorphism, refined map position and exclusion as the Blepharophimosis Ptosis Epicanthus inversus Syndrome gene

Mol Cell Probes. 1998 Aug;12(4):255-8. doi: 10.1006/mcpr.1998.0171.
No abstract available

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Blepharophimosis / genetics*
  • Blepharoptosis / genetics*
  • Chromosome Mapping*
  • Chromosomes, Human, Pair 3
  • Genes*
  • Humans
  • Introns
  • Polymorphism, Genetic*
  • Polymorphism, Single-Stranded Conformational
  • Retinol-Binding Proteins / genetics*
  • Retinol-Binding Proteins, Cellular
  • Syndrome

Substances

  • Retinol-Binding Proteins
  • Retinol-Binding Proteins, Cellular

Grants and funding