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...
Wedi'i Gadw mewn:
| Prif Awduron: | , , , , , |
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| Fformat: | Artigo |
| Iaith: | Inglês |
| Cyhoeddwyd: |
BMJ Group
2007
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| Pynciau: | |
| Mynediad Ar-lein: | 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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