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G2019S LRRK2 mutation causing Parkinson's disease without Lewy bodies
The G2019S leucine‐rich repeat kinase 2 gene (LRRK2) mutation has been identified in a significant proportion of familial and sporadic cases of Parkinson's disease (PD). Until now, information on the neuropathological changes associated with the G2019S LRRK2 mutation has been sparse. We report...
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| Hauptverfasser: | , , , , , |
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| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
BMJ Group
2007
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2077973/ https://ncbi.nlm.nih.gov/pubmed/17210620 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jnnp.2006.107904 |
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