Rare among Rare: Phenotypes of Uncommon CMT Genotypes
(1) Background: Charcot–Marie–Tooth disease (CMT) is the most frequent form of inherited chronic motor and sensory polyneuropathy. Over 100 CMT causative genes have been identified. Previous reports found <i>PMP22</i>, <i>GJB1</i>, <i>MPZ</i>, and <i>MFN2</i> as the most frequently involved genes. O...
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| Główni autorzy: | , , , , , , , , |
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| Format: | Artigo |
| Język: | Inglês |
| Wydane: |
MDPI AG
2021-12-01
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| Seria: | Brain Sciences |
| Hasła przedmiotowe: | |
| Dostęp online: | https://www.mdpi.com/2076-3425/11/12/1616 |
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