Familial Parkinsonism and early onset Parkinson's disease in a Brazilian movement disorders clinic: phenotypic characterization and frequency of SNCA, PRKN, PINK1, and LRRK2 mutations.

Source:http://linkedlifedata.com/resource/pubmed/id/19205068

Mov. Disord. 2009 Apr 15 24 5 662-6

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PMID
19205068