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Recessively inherited parkinsonism: effect of ATP13A2 mutations on the clinical and neuroimaging phenotype

Brüggemann N, Hagenah J, Reetz K, Schmidt A, Kasten M, Buchmann I, Eckerle S, Bähre M, Münchau A, Djarmati A, Van der Vegt J, Siebner H, Binkofski F, Ramirez A, Behrens MI and Klein C

2010

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To determine clinical features and to identify changes in brain structure and function in compound heterozygous and heterozygous ATP13A2 mutation carriers.
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