Recessively inherited parkinsonism: effect of ATP13A2 mutations on the clinical and neuroimaging phenotype.
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Abstract
To determine clinical features and to identify changes in brain structure and function in compound heterozygous and heterozygous ATP13A2 mutation carriers.
Bibliographical data
| Original language | German |
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| Article number | 11 |
| ISSN | 0003-9942 |
| Publication status | Published - 2010 |
| pubmed | 21060012 |
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