SLC25A46 mutations underlie progressive myoclonic ataxia with optic atrophy and neuropathy

Gavin Charlesworth, Bettina Balint, Niccolò E. Mencacci, Lucinda Carr, Nicholas W. Wood, Kailash P. Bhatia*

*Corresponding author for this work

Research output: Contribution to journalLetter

19 Scopus citations
Original languageEnglish (US)
Pages (from-to)1249-1251
Number of pages3
JournalMovement Disorders
Volume31
Issue number8
DOIs
StatePublished - Aug 1 2016

ASJC Scopus subject areas

  • Neurology
  • Clinical Neurology

Cite this

Charlesworth, G., Balint, B., Mencacci, N. E., Carr, L., Wood, N. W., & Bhatia, K. P. (2016). SLC25A46 mutations underlie progressive myoclonic ataxia with optic atrophy and neuropathy. Movement Disorders, 31(8), 1249-1251. https://doi.org/10.1002/mds.26716