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Impaired Differentiation of Schwann Cells in Transgenic Mice with Increased PMP22 Gene Dosage
An intrachromosomal duplication containing the PMP22gene is associated with the human hereditary peripheral neuropathy Charcot-Marie-Tooth disease type 1A, and PMP22 overexpression as a consequence of increased PMP22 gene dosage has been suggested as causative event in this frequent disorder of peri...
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| Publicat a: | J Neurosci |
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| Autors principals: | , , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Society for Neuroscience
1996
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6578876/ https://ncbi.nlm.nih.gov/pubmed/8757248 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1523/JNEUROSCI.16-17-05351.1996 |
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