Lack of G2019S LRRK2 mutation in a cohort of Taiwanese with sporadic Parkinson's disease. [electronic resource]

By: Contributor(s): Producer: 20061114Description: 880-1 p. digitalISSN:
  • 0885-3185
Subject(s): Online resources: In: Movement disorders : official journal of the Movement Disorder Society vol. 21
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Publication Type: Journal Article

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