Patterns of inheritance, not always easily visible

BMJ. 2013 Nov 6:347:f6610. doi: 10.1136/bmj.f6610.
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Child, Preschool
  • Corneal Dystrophies, Hereditary / diagnosis*
  • Corneal Dystrophies, Hereditary / genetics
  • Dimethylallyltranstransferase / genetics*
  • Genotype
  • Humans
  • Inheritance Patterns*
  • Male
  • Mutation / genetics*
  • Pedigree
  • Risk Assessment
  • Sequence Analysis, DNA

Substances

  • Dimethylallyltranstransferase
  • UBIAD1 protein, human

Supplementary concepts

  • Corneal Dystrophy, Crystalline, of Schnyder