The phenotypic manifestations of autosomal recessive axonalCharcot–Marie–Tooth due to a mutation in Lamin A/C gene-Reference-Cited by-同舟云学术

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The phenotypic manifestations of autosomal recessive axonalCharcot–Marie–Tooth due to a mutation in Lamin A/C gene

Published:2003-01 Issue:1 Volume:13 Page:60-67
ISSN:0960-8966
Container-title:Neuromuscular Disorders
language:en
Short-container-title:Neuromuscular Disorders

Author:

Chaouch M.,Allal Y.,De Sandre-Giovannoli A.,Vallat J.M.,Amer-el-Khedoud A.,Kassouri N.,Chaouch A.,Sindou P.,Hammadouche T.,Tazir M.,Lévy N.,Grid D.

Publisher

Elsevier BV

Subject

Genetics (clinical),Neurology (clinical),Neurology,Pediatrics, Perinatology and Child Health

Reference45 articles.

1. Lower motor and sensory neuron diseases with peroneal muscular atrophy. I. Neurologic, genetic and electrophysiologic findings in hereditary polyneuropathies;Dyck;Arch Neurol,1968

2. Lower motor and primary sensory neuron diseases with peroneal muscular atrophy. II. Neurologic, genetic and electrophysiologic findings in various neuronal degenerations;Dyck;Arch Neurol,1968

3. The clinical features of hereditary motor and sensory neuropathy types I and II;Harding;Brain,1980

4. Second workshop of the European CMT consortium: 53rd ENMC international workshop on classification and diagnostic guidelines for Charcot–Marie–Tooth Type 2 (CMT2–HMSN II) and distal hereditary motor neuropathy (distal HMN–spinal CMT), September 26–28, 1997, Naarden, The Netherlands;De Jonghe;Neuromuscul Disord,1998

5. Charcot–Marie–Tooth disease (CMT): distinctive phenotypic and genotypic features in CMT type 2;Gemignani;J Neurol Sci.,2001

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