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...

Full beskrivning

Sparad:
Bibliografiska uppgifter
I publikationen:Eur J Neurol
Huvudupphovsmän: 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.
Materialtyp: Artigo
Språk:Inglês
Publicerad: 2017
Ämnen:
Article
Länkar: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
Taggar: Lägg till en tagg
Inga taggar, Lägg till första taggen!

Liknande verk