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Comparison of a new pmp22 transgenic mouse line with other mouse models and human patients with CMT1A*
Charcot-Marie-Tooth disease type 1A is a dominantly inherited demyelinating disorder of the peripheral nervous system. It is most frequently caused by overexpression of peripheral myelin protein 22 (PMP22), but is also caused by point mutations in the PMP22 gene. We describe a new transgenic mouse m...
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| Main Authors: | , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Blackwell Science Inc
2002
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1570695/ https://ncbi.nlm.nih.gov/pubmed/12090404 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1046/j.1469-7580.2002.00039.x |
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