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Expanding the Spectrum of Movement Disorders Associated With C9orf72 Hexanucleotide Expansions
OBJECTIVE: Hexanucleotide repeat expansions (HREs) in C9orf72 are a major cause of frontotemporal dementia (FTD) and amyotrophic lateral sclerosis (ALS). We aimed to determine the frequency and phenomenology of movement disorders (MD) in carriers of HRE in C9orf72 through a retrospective review of p...
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| Publicat a: | Neurol Genet |
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| Autors principals: | , , , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Wolters Kluwer
2021
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8105892/ https://ncbi.nlm.nih.gov/pubmed/33977144 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1212/NXG.0000000000000575 |
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