The many faces of Charcot-Marie-Tooth disease

被引：31

作者：

Vance, JM ^{[1
]}

机构：

[1] Duke Univ, Med Ctr, Dept Med, Durham, NC 27710 USA

来源：

ARCHIVES OF NEUROLOGY | 2000年 / 57卷 / 05期

关键词：

D O I：

10.1001/archneur.57.5.638

中图分类号：

R74 [神经病学与精神病学];

学科分类号：

摘要：

引用

页码：638 / 640

页数：3

共 17 条

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[2] The Thr124Met mutation in the peripheral myelin protein zero (MPZ) gene is associated with a clinically distinct Charcot-Marie-Tooth phenotype
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[3] LOWER MOTOR AND PRIMARY SENSORY NEURON DISEASES WITH PERONEAL MUSCULAR ATROPHY .2. NEUROLOGIC GENETIC AND ELECTROPHYSIOLOGIC FINDINGS IN VARIOUS NEURONAL DEGENERATIONS
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[J]. ARCHIVES OF NEUROLOGY, 1968, 18 (06) : 619 - &
[4] LOWER MOTOR AND PRIMARY SENSORY NEURON DISEASES WITH PERONEAL MUSCULAR ATROPHY .I. NEUROLOGIC GENETIC AND ELECTROPHYSIOLOGIC FINDINGS IN HEREDITARY POLYNEUROPATHIES
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[5] AUTOSOMAL RECESSIVE FORMS OF HEREDITARY MOTOR AND SENSORY NEUROPATHY
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[6] KWON JM, 1995, AM J HUM GENET, V57, P853
[7] Marrosu MG, 1999, NEUROLOGY, V52, P1111
[8] Hereditary motor and sensory neuropathy type 2C is genetically distinct from types 2B and 2D
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Dyck, PJ
[J]. ARCHIVES OF NEUROLOGY, 2000, 57 (05) : 669 - 672
[9] INTERMEDIATE NERVE-CONDUCTION VELOCITIES DEFINE X-LINKED CHARCOT-MARIE-TOOTH NEUROPATHY FAMILIES
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[J]. NEUROLOGY, 1993, 43 (12) : 2558 - 2564
[10] Pareyson D, 1999, NEUROLOGY, V52, P1110

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