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Upregulation of large myelin protein zero leads to Charcot–Marie–Tooth disease-like neuropathy in mice
Charcot–Marie–Tooth (CMT) disease is a hereditary neuropathy mainly caused by gene mutation of peripheral myelin proteins including myelin protein zero (P0, MPZ). Large myelin protein zero (L-MPZ) is an isoform of P0 that contains an extended polypeptide synthesized by translational readthrough at t...
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| Pubblicato in: | Commun Biol |
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| Autori principali: | , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Nature Publishing Group UK
2020
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7070019/ https://ncbi.nlm.nih.gov/pubmed/32170207 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s42003-020-0854-z |
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