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...

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Bibliografiset tiedot
Julkaisussa:Neurobiol Aging
Päätekijät: 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
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 2016
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Article
Linkit: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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