[Spinocerebellar ataxia-27: description of the clinical phenotype of two twin sisters with a deletion in the FGF14 gene]

Rev Neurol. 2016 Mar 1;62(5):238-9.
[Article in Spanish]
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Child, Preschool
  • Diseases in Twins / genetics*
  • Female
  • Fibroblast Growth Factors / genetics*
  • Humans
  • Phenotype
  • Sequence Deletion*
  • Spinocerebellar Degenerations / diagnosis
  • Spinocerebellar Degenerations / genetics*

Substances

  • fibroblast growth factor 14
  • Fibroblast Growth Factors

Supplementary concepts

  • Spinocerebellar ataxia 27