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C9orf72 mutation is rare in Alzheimer's disease, Parkinson's disease, and essential tremor in China
GGGGCC repeat expansions in the C9orf72 gene have been identified as a major contributing factor in patients with amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD). Given the overlapping of clinical phenotypes and pathological characteristics between these two diseases and Alzhei...
| Autores principales: | , , , , , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Frontiers Media S.A.
2013
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3782144/ https://www.ncbi.nlm.nih.gov/pubmed/24068985 http://dx.doi.org/10.3389/fncel.2013.00164 |