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One Multilocus Genomic Variation Is Responsible for a Severe Charcot–Marie–Tooth Axonal Form
Charcot–Marie–Tooth (CMT) disease is a heterogeneous group of inherited disorders affecting the peripheral nervous system, with a prevalence of 1/2500. So far, mutations in more than 80 genes have been identified causing either demyelinating forms (CMT1) or axonal forms (CMT2). Consequentially, the...
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| Pubblicato in: | Brain Sci |
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| Autori principali: | , , , , , , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
MDPI
2020
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7765239/ https://ncbi.nlm.nih.gov/pubmed/33333791 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/brainsci10120986 |
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