Novel LAMB3 mutations cause non-syndromic amelogenesis imperfecta with variable expressivity

Clin Genet. 2015;87(1):90-2. doi: 10.1111/cge.12340. Epub 2014 Feb 4.
No abstract available

Publication types

  • Case Reports
  • Letter
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amelogenesis Imperfecta / genetics*
  • Amelogenesis Imperfecta / pathology*
  • Base Sequence
  • Cell Adhesion Molecules / genetics*
  • Child
  • Child, Preschool
  • Epidermolysis Bullosa, Junctional / genetics*
  • Female
  • Genes, Dominant / genetics
  • Humans
  • Kalinin
  • Male
  • Molecular Sequence Data
  • Pedigree
  • Sequence Analysis, DNA
  • Tooth / pathology

Substances

  • Cell Adhesion Molecules