Lethal osteogenesis imperfecta and a collagen gene deletion. Length polymorphism provides an alternative explanation

Hum Genet. 1985;70(1):35-7. doi: 10.1007/BF00389455.

Abstract

A 300 base pair deletion near the 3'-end of the gene encoding Type II (cartilage) collagen has been implicated in the pathogenesis of perinatal lethal osteogenesis imperfecta. We have found similar deletions occurring at a high frequency in normal Asian Indian and West Indian populations generated by a length polymorphism just beyond the 3'-end of the gene. We suggest that this polymorphism provides an alternative explanation of the original results.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Base Composition
  • Chromosome Deletion*
  • Collagen / genetics*
  • DNA / genetics*
  • Genes*
  • Heterozygote
  • Humans
  • Osteogenesis Imperfecta / genetics*
  • Polymorphism, Genetic*
  • Risk

Substances

  • Collagen
  • DNA