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pubmed-article:17485642pubmed:abstractTextTo assess the prevalence, nature, and associated phenotypes of ATP13A2 gene mutations among patients with juvenile parkinsonism (onset <21 years) or young onset (between 21 and 40 years) Parkinson disease (YOPD).lld:pubmed
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pubmed-article:17485642pubmed:affiliationDepartment of Clinical Genetics, Erasmus MC, Rotterdam, The Netherlands. v.bonifati@erasmusmc.nllld:pubmed
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