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Clinical and Neuroimaging Features in Charcot–Marie–Tooth Patients with GNB4 Mutations
Charcot–Marie–Tooth disease (CMT) is the most common inherited peripheral neuropathy. Mutations in the GNB4 gene cause dominant intermediate CMT type F (CMTDIF). The aim of this study is to investigate phenotypic heterogeneities and characteristics of CMT patients with GNB4 mutations. We enrolled 11...
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| Publicado no: | Life (Basel) |
|---|---|
| Main Authors: | , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
MDPI
2021
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8227704/ https://ncbi.nlm.nih.gov/pubmed/34071515 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/life11060494 |
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