Loss-of-function mutations in RAB39B are associated with typical early-onset Parkinson disease
Identifieur interne : 000581 ( Main/Curation ); précédent : 000580; suivant : 000582Loss-of-function mutations in RAB39B are associated with typical early-onset Parkinson disease
Auteurs : Suzanne Lesage ; Jose Bras ; Florence Cormier-Dequaire ; Christel Condroyer ; Aude Nicolas ; Lee Darwent ; Rita Guerreiro ; Elisa Majounie ; Monica Federoff ; Peter Heutink ; Nicholas W. Wood ; Thomas Gasser ; John Hardy ; François Tison ; Andrew Singleton ; Alexis BriceSource :
- Neurology: Genetics [ 2376-7839 ] ; 2015.
Url:
DOI: 10.1212/NXG.0000000000000009
PubMed: 27066548
PubMed Central: 4821081
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PMC:4821081Le document en format XML
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