De novo KCNA2 mutations cause hereditary spastic paraplegia.
作者信息
Manole Andreea, Männikkö Roope, Hanna Michael G, Kullmann Dimitri M, Houlden Henry
机构信息
Department of Molecular Neuroscience and Neurogenetics Laboratory, UCL Institute of Neurology, London, United Kingdom.
MRC Centre for Neuromuscular Diseases, UCL Institute of Neurology, London, United Kingdom.
出版信息
Ann Neurol. 2017 Feb;81(2):326-328. doi: 10.1002/ana.24866.
PMID:28032718
Abstract
摘要
Zotero 插件