Loss-of-function mutations in RAB39B are associated with typical early-onset Parkinson disease

Detalles Bibliográficos
Autores principales: Lesage, Suzanne, Bras, Jose, Cormier-Dequaire, Florence, Condroyer, Christel, Nicolas, Aude, Darwent, Lee, Guerreiro, Rita, Majounie, Elisa, Federoff, Monica, Heutink, Peter, Wood, Nicholas W., Gasser, Thomas, Hardy, John, Tison, François, Singleton, Andrew, Brice, Alexis
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer 2015
Materias:
Clinical/Scientific Notes
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4821081/
https://www.ncbi.nlm.nih.gov/pubmed/27066548
http://dx.doi.org/10.1212/NXG.0000000000000009

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4821081/
https://www.ncbi.nlm.nih.gov/pubmed/27066548
http://dx.doi.org/10.1212/NXG.0000000000000009

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