A novel mutation in intron 6 of the SPAST gene is associated with a relatively mild phenotype of pure hereditary spastic paraplegia (HSP)

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作者：
O'Dowd, S. T.
Roberts, K.
Cummins, G.
O'Rourke, K.
Lynch, T.
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MOVEMENT DISORDERS | 2011年 / 26卷
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R74 [神经病学与精神病学];
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1102
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页码：S367 / S367
页数：1
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