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Loss-of-function mutations in RAB39B are associated with typical early-onset Parkinson disease
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer
2015
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Materias: | |
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 |
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author | 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 |
author_facet | 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 |
author_sort | Lesage, Suzanne |
collection | PubMed |
description | |
format | Online Article Text |
id | pubmed-4821081 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Wolters Kluwer |
record_format | MEDLINE/PubMed |
spelling | pubmed-48210812016-04-08 Loss-of-function mutations in RAB39B are associated with typical early-onset Parkinson disease 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 Neurol Genet Clinical/Scientific Notes Wolters Kluwer 2015-06-18 /pmc/articles/PMC4821081/ /pubmed/27066548 http://dx.doi.org/10.1212/NXG.0000000000000009 Text en © 2015 American Academy of Neurology This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (http://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits downloading and sharing the work provided it is properly cited. The work cannot be changed in any way or used commercially. |
spellingShingle | Clinical/Scientific Notes 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 Loss-of-function mutations in RAB39B are associated with typical early-onset Parkinson disease |
title | Loss-of-function mutations in RAB39B are associated with typical early-onset Parkinson disease |
title_full | Loss-of-function mutations in RAB39B are associated with typical early-onset Parkinson disease |
title_fullStr | Loss-of-function mutations in RAB39B are associated with typical early-onset Parkinson disease |
title_full_unstemmed | Loss-of-function mutations in RAB39B are associated with typical early-onset Parkinson disease |
title_short | Loss-of-function mutations in RAB39B are associated with typical early-onset Parkinson disease |
title_sort | loss-of-function mutations in rab39b are associated with typical early-onset parkinson disease |
topic | Clinical/Scientific Notes |
url | 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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