SLC25A46 mutations underlie progressive myoclonic ataxia with optic atrophy and neuropathy.
作者信息
Charlesworth Gavin, Balint Bettina, Mencacci Niccolò E, Carr Lucinda, Wood Nicholas W, Bhatia Kailash P
机构信息
Department of Molecular Neuroscience, UCL Institute of Neurology, Queen Square, London, United Kingdom.
Sobell Department of Motor Neuroscience and Movement Disorders UCL Institute of Neurology, London, United Kingdom.
出版信息
Mov Disord. 2016 Aug;31(8):1249-51. doi: 10.1002/mds.26716. Epub 2016 Jul 19.
PMID:27430653
Abstract
摘要
Zotero 插件