Novel mutations in SPG11 cause hereditary spastic paraplegia associated with early-onset levodopa-responsive Parkinsonism (Q59153436)
scientific article published on 01 February 2011
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Current Data About Novel mutations in SPG11 cause hereditary spastic paraplegia associated with early-onset levodopa-responsive Parkinsonism
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(P1932) Filippo M Santorelli
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(P1476) "Novel mutations in SPG11 cause hereditary spastic paraplegia associated with early-onset levodopa-responsive Parkinsonism" (language: en)
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(P2093) Arianna Guidubaldi
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Martina Petracca
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Alessandra Tessa
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other details
description scientific article published on 01 February 2011

External Links
(P356) 10.1002/MDS.23552
(P698) 21381113