Abstract
The discovery of mutations that contribute to movement disorders has facilitated the identification of converging pathways and novel therapeutic targets. Successful translation of these research findings into clinical practice will require identification of early markers of disease progression, and recent research indicates that progress is being made in this area.
| Original language | English |
|---|---|
| Journal | Nature Reviews Neurology |
| Volume | 8 |
| Issue number | 2 |
| Pages (from-to) | 65-66 |
| Number of pages | 2 |
| ISSN | 1759-4758 |
| DOIs | |
| Publication status | Published - 02.2012 |
Funding
C. Klein is funded by a career development award from the Hermann and Lilly Schilling Foundation. D. Krainc is supported by the National Institute of Neurological Disorders and Stroke and the CHDI Foundation.
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
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