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SCIENTIFIC LITERATURE · MED

Novel mutation in ATP13A2 widens the spectrum of Kufor-Rakeb syndrome (PARK9).

Clin Genet · 2011-07-18

DOI: 10.1111/j.1399-0004.2011.01745.xPMID: 21696388

Check source for accessResearch Support, Non-U.S. Gov't; Journal ArticleOriginal source ↗

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