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Refinado por: Base de dados/Biblioteca: IngentaConnect Journals remover Nome da Publicação: Neurology. Genetics remover Neurology remover
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Loss-of-function mutations in RAB39B are associated with typical early-onset Parkinson disease
Loss-of-function mutations in RAB39B are associated with typical early-onset Parkinson disease
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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

Neurology, 2015-06, Vol.1 (1), p.e9-e9 [Periódico revisado por pares]

United States: American Academy of Neurology

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  • Realização: ABCD-USP USP   Logos de Redes Sociais: Freepik

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