A novel FGF8 mutation in a female patient with isolated congenital anosmia

Hormones (Athens). 2019 Jun;18(2):241-244. doi: 10.1007/s42000-019-00108-6. Epub 2019 May 13.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Child
  • Female
  • Fibroblast Growth Factor 8 / genetics*
  • Fibroblast Growth Factor 8 / metabolism*
  • Gene Expression Regulation, Developmental
  • Genetic Predisposition to Disease*
  • Humans
  • Magnetic Resonance Angiography
  • Mutation*
  • Olfaction Disorders / congenital*
  • Olfaction Disorders / genetics*
  • Olfactory Bulb / diagnostic imaging
  • Olfactory Bulb / pathology

Substances

  • FGF8 protein, human
  • Fibroblast Growth Factor 8