Two novel bi-allelic KDELR2 missense variants cause osteogenesis imperfecta with neurodevelopmental features

Am J Med Genet A. 2021 Jul;185(7):2241-2249. doi: 10.1002/ajmg.a.62221. Epub 2021 May 8.
No abstract available

Publication types

  • Letter
  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alleles
  • Child
  • Child, Preschool
  • Female
  • Genetic Predisposition to Disease*
  • Humans
  • Male
  • Mutation, Missense / genetics
  • Neurodevelopmental Disorders / genetics*
  • Neurodevelopmental Disorders / physiopathology
  • Osteogenesis Imperfecta / genetics*
  • Osteogenesis Imperfecta / physiopathology
  • Vesicular Transport Proteins / genetics*

Substances

  • Vesicular Transport Proteins
  • KDELR2 protein, human