| Autor: |
Winkler, S, Hagenah, J, Lincoln, S, Heckman, M, Haugarvoll, K, Lohmann-Hedrich, K, Kostic, V, Farrer, M, Klein, C |
| Zdroj: |
Neurology (Ovid); October 2007, Vol. 69 Issue: 18 p1745-1750, 6p |
| Abstrakt: |
Mutations in the -synuclein(SNCA) gene have been shown to be responsible for a rare familial form of Parkinson disease (PD). Furthermore, polymorphic variants in multiple regions of the gene have been associated with susceptibility to idiopathic PD in different populations. |
| Databáze: |
Supplemental Index |
| Externí odkaz: |
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