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Understanding Schwann cell–neurone interactions: the key to Charcot–Marie–Tooth disease?*
Charcot–Marie–Tooth disease (CMT) comprises a heterogeneous group of disorders. The most frequent subtype is caused by increased PMP22 gene dosage or missense point mutations affecting the PMP22 gene (CMT type 1A; CMT1A). Animal models in rat and mouse with the corresponding PMP22 alterations are av...
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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/PMC1570699/ https://ncbi.nlm.nih.gov/pubmed/12090402 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1046/j.1469-7580.2002.00044.x |
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