GBA mutations in Parkinson disease: Earlier death but similar neuropathological features

BACKGROUND: Mutations in the glucocerebrosidase (GBA) gene are known to be a risk factor for Parkinson’s disease (PD). Data on clinicopathologic correlation is limited. The purpose of this study was to determine the clinicopathological findings that might distinguish PD cases with and without mutati...

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Detalhes bibliográficos
Publicado no:Eur J Neurol
Main Authors: Adler, Charles H., Beach, Thomas G., Shill, Holly A., Caviness, John N., Driver-Dunckley, Erika, Sabbagh, Marwan N., Patel, Akta, Sue, Lucia I., Serrano, Geidy, Jacobson, Sandra A., Davis, Kathryn, Belden, Christine M., Dugger, Brittany N., Paciga, Sara A., Winslow, Ashley R., Hirst, Warren D., Hentz, Joseph G.
Formato: Artigo
Idioma:Inglês
Publicado em: 2017
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5657539/
https://ncbi.nlm.nih.gov/pubmed/28834018
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/ene.13395
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