Atypical hereditary spastic paraplegia with thin corpus callosum in a Korean patient with a novel SPG11 mutation. [electronic resource]

By: Contributor(s): Producer: 20120406Description: e7-8 p. digitalISSN:
  • 1468-1331
Subject(s): Online resources: In: European journal of neurology vol. 19
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Publication Type: Case Reports; Letter

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