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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DOI：
10.1212/nxg.0000000000000009
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发表时间：
2015-06
期刊：
影响因子：
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通讯作者：
French Parkinson's Disease Genetics Study Group (PDG) and the International Parkinson's Disease Genomics Consortium (IPDGC)
中科院分区：
文献类型：
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作者：
Lesage S;Bras J;Cormier-Dequaire F;Condroyer C;Nicolas A;Darwent L;Guerreiro R;Majounie E;Federoff M;Heutink P;Wood NW;Gasser T;Hardy J;Tison F;Singleton A;Brice A;French Parkinson's Disease Genetics Study Group (PDG) and the International Parkinson's Disease Genomics Consortium (IPDGC)
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