Motor and sensory neuropathy due to myelin infolding and paranodal damage in a transgenic mouse model of Charcot–Marie–Tooth disease type 1C-Reference-Cited by-同舟云学术

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Motor and sensory neuropathy due to myelin infolding and paranodal damage in a transgenic mouse model of Charcot–Marie–Tooth disease type 1C

Published:2013-01-28 Issue:9 Volume:22 Page:1755-1770
ISSN:1460-2083
Container-title:Human Molecular Genetics
language:en
Short-container-title:

Author:

Lee Samuel M.,Sha Di,Mohammed Anum A.,Asress Seneshaw,Glass Jonathan D.,Chin Lih-Shen,Li Lian

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/22/9/1755/14140969/ddt022.pdf

Reference49 articles.

1. Diagnosis, natural history, and management of Charcot-Marie-Tooth disease;Pareyson;Lancet Neurol.,2009

2. Update on Charcot-Marie-Tooth disease;Patzko;Curr. Neurol. Nuerosci. Rep.,2011

3. Estimation of the mutation frequencies in Charcot-Marie-Tooth disease type 1 and hereditary neuropathy with liability to pressure palsies: a European collaborative study;Nelis;Eur. J. Hum. Genet.,1996

4. SIMPLE mutation in demyelinating neuropathy and distribution in sciatic nerve;Bennett;Ann. Neurol.,2004

5. SIMPLE mutations in Charcot-Marie-Tooth disease and the potential role of its protein product in protein degradation;Saifi;Hum. Mutat.,2005

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1. Conduction slowing, conduction block and temporal dispersion in demyelinating, dysmyelinating and axonal neuropathies: Electrophysiology meets pathology;Journal of the Peripheral Nervous System;2024-04-10

2. Identification and clinical characterization of Charcot-Marie-Tooth disease type 1C patients with LITAF p.G112S mutation;Genes & Genomics;2022-05-24

3. PLEKHG5-related autosomal recessive lower motor neuron disease with dysmyelination in peripheral nerves;Clinical Neuropathology;2021-11-01

4. Animal Models as a Tool to Design Therapeutical Strategies for CMT-like Hereditary Neuropathies;Brain Sciences;2021-09-18

5. New evidence for secondary axonal degeneration in demyelinating neuropathies;Neuroscience Letters;2021-01

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