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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
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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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