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Axonal Charcot-Marie-tooth disease - The fog is slowly lifting
被引:12
作者
:
Reilly, MM
论文数:
0
引用数:
0
h-index:
0
机构:
UCL Natl Hosp Neurol & Neurosurg, Inst Neurol, Ctr Neuromuscular Dis, London WC1N 3BG, England
Reilly, MM
机构
:
[1]
UCL Natl Hosp Neurol & Neurosurg, Inst Neurol, Ctr Neuromuscular Dis, London WC1N 3BG, England
[2]
UCL Natl Hosp Neurol & Neurosurg, Inst Neurol, Dept Mol Neurosci, London WC1N 3BG, England
来源
:
NEUROLOGY
|
2005年
/ 65卷
/ 02期
关键词
:
D O I
:
10.1212/01.wnl.0000173904.97549.94
中图分类号
:
R74 [神经病学与精神病学];
学科分类号
:
摘要
:
引用
收藏
页码:186 / 187
页数:2
相关论文
共 7 条
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Glycyl tRNA synthetase mutations in Charcot-Marie-Tooth disease type 2D and distal spinal muscular atrophy type V
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NINDS, Neurogenet Branch, NIH, Bethesda, MD 20892 USA
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机构:
NINDS, Neurogenet Branch, NIH, Bethesda, MD 20892 USA
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Goldfarb, LG
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机构:
NINDS, Neurogenet Branch, NIH, Bethesda, MD 20892 USA
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h-index:
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机构:
Yamagata Univ, Sch Med, Dept Pediat, Yamagata 9909585, Japan
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0
引用数:
0
h-index:
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机构:
Yamagata Univ, Sch Med, Dept Pediat, Yamagata 9909585, Japan
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h-index:
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机构:
Yamagata Univ, Sch Med, Dept Pediat, Yamagata 9909585, Japan
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机构:
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Mayo Clin & Mayo Fdn, Peripheral Neuropathy Res Lab, Rochester, MI USA
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Mayo Clin & Mayo Fdn, Peripheral Neuropathy Res Lab, Rochester, MI USA
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Mayo Clin & Mayo Fdn, Peripheral Neuropathy Res Lab, Rochester, MI USA
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Mayo Clin & Mayo Fdn, Peripheral Neuropathy Res Lab, Rochester, MI USA
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0
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Duke Univ, Med Ctr, Ctr Human Genet, Durham, NC 27710 USA
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Zappia, M
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0
引用数:
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Duke Univ, Med Ctr, Ctr Human Genet, Durham, NC 27710 USA
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0
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0
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0
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0
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0
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Duke Univ, Med Ctr, Ctr Human Genet, Durham, NC 27710 USA
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0
引用数:
0
h-index:
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Duke Univ, Med Ctr, Ctr Human Genet, Durham, NC 27710 USA
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Parman, Y
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0
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Duke Univ, Med Ctr, Ctr Human Genet, Durham, NC 27710 USA
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Evgrafov, O
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0
引用数:
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机构:
Duke Univ, Med Ctr, Ctr Human Genet, Durham, NC 27710 USA
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De Jonghe, P
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0
引用数:
0
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机构:
Duke Univ, Med Ctr, Ctr Human Genet, Durham, NC 27710 USA
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Takahashi, Y
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0
引用数:
0
h-index:
0
机构:
Duke Univ, Med Ctr, Ctr Human Genet, Durham, NC 27710 USA
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0
引用数:
0
h-index:
0
机构:
Duke Univ, Med Ctr, Ctr Human Genet, Durham, NC 27710 USA
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Pericak-Vance, MA
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0
引用数:
0
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Duke Univ, Med Ctr, Ctr Human Genet, Durham, NC 27710 USA
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Quattrone, A
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Duke Univ, Med Ctr, Ctr Human Genet, Durham, NC 27710 USA
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Duke Univ, Med Ctr, Ctr Human Genet, Durham, NC 27710 USA
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Duke Univ, Med Ctr, Ctr Human Genet, Durham, NC 27710 USA
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Duke Univ, Med Ctr, Ctr Human Genet, Durham, NC 27710 USA
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1
→
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[1]
Glycyl tRNA synthetase mutations in Charcot-Marie-Tooth disease type 2D and distal spinal muscular atrophy type V
[J].
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论文数:
0
引用数:
0
h-index:
0
机构:
NINDS, Neurogenet Branch, NIH, Bethesda, MD 20892 USA
Antonellis, A
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Ellsworth, RE
论文数:
0
引用数:
0
h-index:
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机构:
NINDS, Neurogenet Branch, NIH, Bethesda, MD 20892 USA
Ellsworth, RE
;
Sambuughin, N
论文数:
0
引用数:
0
h-index:
0
机构:
NINDS, Neurogenet Branch, NIH, Bethesda, MD 20892 USA
Sambuughin, N
;
Puls, I
论文数:
0
引用数:
0
h-index:
0
机构:
NINDS, Neurogenet Branch, NIH, Bethesda, MD 20892 USA
Puls, I
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Abel, A
论文数:
0
引用数:
0
h-index:
0
机构:
NINDS, Neurogenet Branch, NIH, Bethesda, MD 20892 USA
Abel, A
;
Lee-Lin, SQ
论文数:
0
引用数:
0
h-index:
0
机构:
NINDS, Neurogenet Branch, NIH, Bethesda, MD 20892 USA
Lee-Lin, SQ
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论文数:
引用数:
h-index:
机构:
Jordanova, A
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Kremensky, I
论文数:
0
引用数:
0
h-index:
0
机构:
NINDS, Neurogenet Branch, NIH, Bethesda, MD 20892 USA
Kremensky, I
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论文数:
引用数:
h-index:
机构:
Christodoulou, K
;
Middleton, LT
论文数:
0
引用数:
0
h-index:
0
机构:
NINDS, Neurogenet Branch, NIH, Bethesda, MD 20892 USA
Middleton, LT
;
Sivakumar, K
论文数:
0
引用数:
0
h-index:
0
机构:
NINDS, Neurogenet Branch, NIH, Bethesda, MD 20892 USA
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Ionasescu, V
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0
引用数:
0
h-index:
0
机构:
NINDS, Neurogenet Branch, NIH, Bethesda, MD 20892 USA
Ionasescu, V
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Funalot, B
论文数:
0
引用数:
0
h-index:
0
机构:
NINDS, Neurogenet Branch, NIH, Bethesda, MD 20892 USA
Funalot, B
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Vance, JM
论文数:
0
引用数:
0
h-index:
0
机构:
NINDS, Neurogenet Branch, NIH, Bethesda, MD 20892 USA
Vance, JM
;
Goldfarb, LG
论文数:
0
引用数:
0
h-index:
0
机构:
NINDS, Neurogenet Branch, NIH, Bethesda, MD 20892 USA
Goldfarb, LG
;
Fischbeck, KH
论文数:
0
引用数:
0
h-index:
0
机构:
NINDS, Neurogenet Branch, NIH, Bethesda, MD 20892 USA
Fischbeck, KH
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论文数:
引用数:
h-index:
机构:
Green, ED
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AMERICAN JOURNAL OF HUMAN GENETICS,
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72
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[2]
Mitochondrial GTPase mitofusin 2 mutation in Charcot-Marie-Tooth neuropathy type 2A
[J].
Kijima, K
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0
引用数:
0
h-index:
0
机构:
Yamagata Univ, Sch Med, Dept Pediat, Yamagata 9909585, Japan
Kijima, K
;
Numakura, C
论文数:
0
引用数:
0
h-index:
0
机构:
Yamagata Univ, Sch Med, Dept Pediat, Yamagata 9909585, Japan
Numakura, C
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Izumino, H
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0
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机构:
Yamagata Univ, Sch Med, Dept Pediat, Yamagata 9909585, Japan
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Umetsu, K
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0
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机构:
Yamagata Univ, Sch Med, Dept Pediat, Yamagata 9909585, Japan
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Nezu, A
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h-index:
0
机构:
Yamagata Univ, Sch Med, Dept Pediat, Yamagata 9909585, Japan
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Shiiki, T
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