Research Watch, Litigation Watch: Welding Rods, Oct. 2004





ARTICLE: "Presence of Spinocerebellar Ataxia Type 2 Gene Mutation in a Patient With Apparently Sporadic Parkinson's disease: Clinical Implications." AUTHORS: D.E. Shan, R.S. Liu, C.M. Sun, S.J. Lee, K.K. Liao, B.W. Soong. JOURNAL: Movement Disorders 2004 Sep 17 [Epub ahead of print] SUMMARY: Among 242 patients with apparently sporadic Parkinson's disease, a 70-year-old man with a CAG repeat number of 37 in the SCA2 gene was identified. The patient remained responsive to levodopa 14 years after the onset and had …





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