| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 10746148 | Parkinsonism & Related Disorders | 2012 | 5 Pages |
Abstract
A compound heterozygous mutation in the ATP13A2 gene is associated with increased intracortical inhibition. In addition, some aspects of interhemispheric inhibition are increased in the presence of a single ATP13A2 mutation.
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Authors
S. Zittel, J. Kroeger, J.P.M. van der Vegt, H.R. Siebner, N. Brüggemann, A. Ramirez, M.I. Behrens, C. Gerloff, T. Bäumer, C. Klein, A. Münchau,