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3. Novel mutations in SPG11 cause hereditary spastic paraplegia associated with early-onset levodopa-responsive Parkinsonism. Guidubaldi A; Piano C; Santorelli FM; Silvestri G; Petracca M; Tessa A; Bentivoglio AR Mov Disord; 2011 Feb; 26(3):553-6. PubMed ID: 21381113 [TBL] [Abstract][Full Text] [Related]
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