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SLC25A46 mutations underlie progressive myoclonic ataxia with optic atrophy and neuropathy

Gavin Charlesworth1, Bettina Balint2,3, Niccolò E Mencacci1

  • 1Department of Molecular Neuroscience, UCL Institute of Neurology, Queen Square, London, United Kingdom.

Movement Disorders : Official Journal of the Movement Disorder Society
|July 20, 2016
PubMed
Abstract

No abstract available in PubMed .

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