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C9orf72 mutation is rare in Alzheimer's disease, Parkinson's disease, and essential tremor in China

1 Jan 2013

Abstract excerpt

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 Alzheimer's disease (AD), Parkinson's disease (PD), and essential tremor (ET), we speculated regarding whether C9orf72...

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Amyotrophic Lateral Sclerosis Research
Genetic Neurodegenerative Diseases
Parkinson's Disease Mechanisms and Treatments

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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PMID: 24068985
DOI: 10.3389/fncel.2013.00164

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