Llwytho...
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 a 77-...
Wedi'i Gadw mewn:
| Prif Awduron: | , , , , , |
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| Fformat: | Artigo |
| Iaith: | Inglês |
| Cyhoeddwyd: |
BMJ Publishing Group
2009
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| Pynciau: | |
| Mynediad Ar-lein: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3029537/ https://ncbi.nlm.nih.gov/pubmed/21686713 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/bcr.08.2008.0632 |
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