Phenotypic Consequences of PLOD2 Mutations in Bruck Syndrome Inform a Collagen Lysyl Hydroxylase Crystal Structure

J Bone Miner Res. 2018 Jul;33(7):1376. doi: 10.1002/jbmr.3459. Epub 2018 Jun 7.
No abstract available

Publication types

  • Letter
  • Comment

MeSH terms

  • Humans
  • Mutation
  • Osteogenesis Imperfecta*
  • Phenotype
  • Procollagen-Lysine, 2-Oxoglutarate 5-Dioxygenase*

Substances

  • PLOD2 protein, human
  • Procollagen-Lysine, 2-Oxoglutarate 5-Dioxygenase