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SLC25A46 mutations underlie progressive myoclonic ataxia with optic atrophy and neuropathy
Charlesworth, Gavin, Balint, Bettina, Mencacci, Niccolò E., Carr, Lucinda, Wood, Nicholas W., Bhatia, Kailash P.Volume:
31
Language:
english
Journal:
Movement Disorders
DOI:
10.1002/mds.26716
Date:
August, 2016
File:
PDF, 232 KB
english, 2016