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The function of the Periaxin gene during nerve repair in a model of CMT4F *
Mutations in the Periaxin (PRX) gene are known to cause autosomal recessive demyelinating Charcot-Marie-Tooth (CMT4F) and Dejerine-Sottas disease. The pathogenesis of these diseases is not fully understood. However, progress is being made by studying both the periaxin-null mouse, a mouse model of th...
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| Main Authors: | , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Blackwell Science Inc
2002
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| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1570694/ https://ncbi.nlm.nih.gov/pubmed/12090399 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1046/j.1469-7580.2002.00038.x |
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