Interesting clinical features associated with mutations in the SLC20A2 gene

被引：0
|
作者：
Schottlaender, L. V. [1 ]
Mencacci, N. [1 ]
Koepp, M. [2 ]
Hanna, M. [3 ]
Hardy, J. [1 ,4 ]
Lees, A. J. [4 ]
Houlden, H. [1 ,3 ]
机构：
[1] UCL Inst Neurol, Dept Mol Neurosci, London, England
[2] Natl Hosp Neurol & Neurosurg, Dept Clin & Expt Epilepsy, London WC1N 3BG, England
[3] UCL, Inst Neurol, Med Res Council Ctr Neuromuscular Dis, Dept Mol Neurosci, London, England
[4] UCL, IoN, Reta Lila Weston Inst Neurol Studies, London, England
来源：
EUROPEAN JOURNAL OF NEUROLOGY | 2012年 / 19卷
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中图分类号：
R74 [神经病学与精神病学];
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摘要：
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页码：40 / 40
页数：1
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