The repeat variant in MSH3 is not a genetic modifier for spinocerebellar ataxia type 3 and Friedreich's ataxia

Brain. 2020 Apr 1;143(4):e25. doi: 10.1093/brain/awaa043.
No abstract available

Publication types

  • Research Support, Non-U.S. Gov't
  • Comment

MeSH terms

  • Friedreich Ataxia*
  • Humans
  • Machado-Joseph Disease*
  • MutS Homolog 3 Protein
  • Myotonic Dystrophy*
  • Phenotype
  • Trinucleotide Repeats

Substances

  • MSH3 protein, human
  • MutS Homolog 3 Protein