Phenotypic variability of TTR Val122Ile mutation: a Caucasian patient with axonal neuropathy and normal heart

Neurol Sci. 2017 Mar;38(3):525-526. doi: 10.1007/s10072-016-2767-7. Epub 2016 Nov 12.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Aged
  • Humans
  • Male
  • Mutation
  • Peripheral Nervous System Diseases / genetics*
  • Peripheral Nervous System Diseases / physiopathology
  • Phenotype
  • Prealbumin / genetics*
  • White People / genetics

Substances

  • Prealbumin