Novel homozygous KREMEN1 mutation causes ectodermal dysplasia

Oral Dis. 2022 Apr;28(3):843-845. doi: 10.1111/odi.13921. Epub 2021 Jun 9.
No abstract available

Keywords: KREMEN1; ectodermal dysplasia; mutation; oligodontia; syndromic.

Publication types

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

MeSH terms

  • Anodontia* / genetics
  • Ectodermal Dysplasia* / genetics
  • Humans
  • Membrane Proteins* / genetics
  • Mutation

Substances

  • KREMEN1 protein, human
  • Membrane Proteins