Hereditory Sensory Neuropathy Type 1 (SPTLC1): phenotypic variation in patients with the English founder mutation

被引：0

作者：

Kugathasan, U. ^{[1
]}

Laura, M. ^{[1
]}

Tomaselli, P. J. ^{[1
]}

Evans, M. R. B. ^{[1
,2
]}

Pittmann, A. ^{[3
]}

Sinclair, C. J. D. ^{[2
]}

Hornemann, T. ^{[4
]}

Suriyanarayanan, S. ^{[4
]}

Phadke, R. ^{[5
]}

Lauria, G. ^{[6
]}

Lombardi, R. ^{[6
]}

Polke, J. M. ^{[7
]}

Bennett, D. L. ^{[8
]}

Houlden, H. ^{[1
]}

Blake, J. ^{[9
]}

Reilly, M. M. ^{[1
]}

机构：

[1] UCL Inst Neurol, MRC Ctr Neuromuscular Dis, London, England

[2] UCL Inst Neurol, Acad Neuroradiol Unit, Dept Brain Repair & Rehabil, London, England

[3] UCL Inst Neurol, London, England

[4] Univ Hosp Zurich, Inst Clin Chem, Zurich, Switzerland

[5] Natl Hosp Neurol & Neurosurg, Div Neuropathol, London, England

[6] IRCCS Fdn, Neurol Unit 3, Carlo Besta Neurol Inst, Milan, Italy

[7] Natl Hosp Neurol & Neurosurg, Neurogenet Unit, London, England

[8] Nuffield Dept Clin Neurosci, Oxford, England

[9] Norfolk & Norwich Univ Hosp, Dept Clin Neurophysiol, Norwich, Norfolk, England

来源：

NEUROMUSCULAR DISORDERS | 2017年 / 27卷

关键词：

D O I：

暂无

中图分类号：

R74 [神经病学与精神病学];

学科分类号：

摘要：

PN09

引用

页码：S26 / S27

页数：2

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