The analysis of C9orf72 repeat expansions in a large series of clinically and pathologically diagnosed cases with atypical parkinsonism()

A GGGGCC repeat expansion in the C9orf72 gene was recently identified as a major cause of familial and sporadic amyotrophic lateral sclerosis and frontotemporal dementia. There is suggestion that these expansions may be a rare cause of parkinsonian disorders such as progressive supranuclear palsy (P...

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Detalles Bibliográficos
Autores principales: Schottlaender, Lucia V., Polke, James M., Ling, Helen, MacDoanld, Nicola D., Tucci, Arianna, Nanji, Tina, Pittman, Alan, de Silva, Rohan, Holton, Janice L., Revesz, Tamas, Sweeney, Mary G., Singleton, Andy B., Lees, Andrew J., Bhatia, Kailash P., Houlden, Henry
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2015
Materias:
Genetic Report Abstract
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4321829/
https://www.ncbi.nlm.nih.gov/pubmed/25308964
http://dx.doi.org/10.1016/j.neurobiolaging.2014.08.024

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4321829/
https://www.ncbi.nlm.nih.gov/pubmed/25308964
http://dx.doi.org/10.1016/j.neurobiolaging.2014.08.024

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