CLINICAL FEATURES AND GENETIC FINDINGS IN PATIENTS WITH CHARCOT MARIE TOOTH DISEASE TYPE 2 (CMT2) DUE TO LRSAM1 MUTATION

被引：0
|
作者：
Cortese, A. [1 ]
Laura, M. [1 ]
Polke, J. M. [2 ]
Rossor, A. M. [1 ]
Tomaselli, P. [1 ]
Blake, J. [1 ]
Poh, R. [2 ]
Lunn, M. [1 ]
Houlden, H. [3 ,4 ]
Reilly, M. M. [1 ]
机构：
[1] Natl Hosp Neurol & Neurosurg, MRC Ctr Neuromuscular Dis, UCL Inst Neurol, Queen Sq, London WC1N 3BG, England
[2] Natl Hosp Neurol & Neurosurg, Dept Neurogenet, UCL Inst Neurol, London, England
[3] UCL Inst Neurol, Dept Mol Neurosci, London, England
[4] Natl Hosp Neurol & Neurosurg, Queen Sq, London, England
来源：
JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM | 2017年 / 22卷
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R74 [神经病学与精神病学];
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摘要：
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页码：S12 / S12
页数：1
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