Analysis of the C9orf72 repeat in Parkinson’s disease, essential tremor and restless legs syndrome

The hexanucleotide expanded repeat (GGGGCC) in intron 1 of the C9orf72 gene is recognized as the most common genetic form of amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD). However, as part of the clinical phenotype, some patients present with parkinsonism. The present study i...

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Detalhes bibliográficos
Main Authors: DeJesus-Hernandez, Mariely, Rayaprolu, Sruti, Soto-Ortolaza, Alexandra I., Rutherford, Nicola J., Heckman, Michael G., Traynor, Sharleen, Strongosky, Audrey, Graff-Radford, Neill, Van Gerpen, Jay, Uitti, Ryan J., Shih, Jerry J., Lin, Siong-Chi, Wszolek, Zbigniew K., Rademakers, Rosa, Ross, Owen A.
Formato: Artigo
Idioma:Inglês
Publicado em: 2012
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3570692/
https://ncbi.nlm.nih.gov/pubmed/23084342
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.parkreldis.2012.09.013
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