Φορτώνει......
An essential role of MAG in mediating axon-myelin attachment in Charcot-Marie-Tooth 1A disease
Charcot-Marie-Tooth disease type 1A (CMT1A) is a hereditary demyelinating peripheral neuropathy caused by the duplication of the PMP22 gene. Demyelination precedes the occurrence of clinical symptoms that correlate with axonal degeneration. It was postulated that a disturbed axon-glia interface cont...
Αποθηκεύτηκε σε:
| Κύριοι συγγραφείς: | , , , , , , , , , |
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| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
2012
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| Θέματα: | |
| Διαθέσιμο Online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3612363/ https://ncbi.nlm.nih.gov/pubmed/22940629 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.nbd.2012.08.009 |
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