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Shortened internodal length of dermal myelinated nerve fibres in Charcot–Marie-Tooth disease type 1A
Charcot–Marie-Tooth disease type 1A is the most common inherited neuropathy and is caused by duplication of chromosome 17p11.2 containing the peripheral myelin protein-22 gene. This disease is characterized by uniform slowing of conduction velocities and secondary axonal loss, which are in contrast...
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| 主要な著者: | , , , , , |
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| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Oxford University Press
2009
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2800385/ https://ncbi.nlm.nih.gov/pubmed/19923170 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/brain/awp274 |
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