Autosomal recessive cerebellar ataxia 3 due to homozygote c.132dupA mutation within the ANO10 gene--reply

JAMA Neurol. 2015 Feb;72(2):239-40. doi: 10.1001/jamaneurol.2014.3921.
No abstract available

Publication types

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

MeSH terms

  • Brain / pathology*
  • Female
  • Humans
  • Male
  • Membrane Proteins / genetics*
  • Spinocerebellar Degenerations / genetics*

Substances

  • Membrane Proteins