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Impaired Mitochondrial Mobility in Charcot-Marie-Tooth Disease
Charcot-Marie-Tooth (CMT) disease is a progressive, peripheral neuropathy and the most commonly inherited neurological disorder. Clinical manifestations of CMT mutations are typically limited to peripheral neurons, the longest cells in the body. Currently, mutations in at least 80 different genes ar...
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| 發表在: | Front Cell Dev Biol |
|---|---|
| Main Authors: | , , |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
Frontiers Media S.A.
2021
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| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7882694/ https://ncbi.nlm.nih.gov/pubmed/33598463 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fcell.2021.624823 |
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