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Unravelling the clinical spectrum and the role of repeat length in C9ORF72 repeat expansions
Since the discovery of the C9orf72 repeat expansion as the most common genetic cause of frontotemporal dementia (FTD) and amyotrophic lateral sclerosis, it has increasingly been associated with a wider spectrum of phenotypes, including other types of dementia, movement disorders, psychiatric symptom...
Guardado en:
| Publicado en: | J Neurol Neurosurg Psychiatry |
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| Autores principales: | , , , , , |
| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
BMJ Publishing Group
2021
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| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8053328/ https://ncbi.nlm.nih.gov/pubmed/33452054 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jnnp-2020-325377 |
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