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c-Jun activation in Schwann cells protects against loss of sensory axons in inherited neuropathy
Charcot–Marie–Tooth disease type 1A is the most frequent inherited peripheral neuropathy. It is generally due to heterozygous inheritance of a partial chromosomal duplication resulting in over-expression of PMP22. A key feature of Charcot–Marie–Tooth disease type 1A is secondary death of axons. Prev...
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| Main Authors: | , , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Oxford University Press
2014
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4208468/ https://ncbi.nlm.nih.gov/pubmed/25216747 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/brain/awu257 |
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