RAB39B gene mutations are not a common cause of Parkinson’s disease or dementia with Lewy bodies

Mutations in Ras-related protein Rab-39B (RAB39B) gene have been linked to X-linked early-onset Parkinsonism with intellectual disabilities. The aim of this study was to address the genetic contribution of RAB39B to Parkinson’s disease (PD), dementia with Lewy bodies (DLB), and pathologically confir...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:Neurobiol Aging
Prif Awduron: Hodges, Kyndall, Brewer, Sheridan S., Labbé, Catherine, Soto-Ortolaza, Alexandra I., Walton, Ronald L., Strongosky, Audrey J., Uitti, Ryan J., van Gerpen, Jay A., Ertekin-Taner, Nilüfer, Kantarci, Kejal, Lowe, Val J., Parisi, Joseph E., Savica, Rodolfo, Graff-Radford, Jonathan, Jones, David T., Knopman, David S., Petersen, Ronald C., Murray, Melissa E., Graff-Radford, Neill R., Ferman, Tanis J., Dickson, Dennis W., Wszolek, Zbigniew K., Boeve, Bradley F., Ross, Owen A., Lorenzo-Betancor, Oswaldo
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: 2016
Pynciau:
Article
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC5954832/
https://ncbi.nlm.nih.gov/pubmed/27459931
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.neurobiolaging.2016.03.021
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