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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Autors principals: 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.
Format: Artigo
Idioma:Inglês
Publicat: 2012
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Article
Accés en línia: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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