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Prevalence of the LRRK2 G2019S mutation in a UK community based idiopathic Parkinson's disease cohort
The LRRK2 G2019S mutation is the commonest genetic cause of Parkinson's disease (PD) identified to date, although estimates of its prevalence in idiopathic disease vary considerably. Our objectives were to determine G2019S mutation frequency in an unselected, community based cohort of idiopathi...
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| Hauptverfasser: | , , , , , , , , |
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| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
BMJ Group
2006
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2117467/ https://ncbi.nlm.nih.gov/pubmed/16614029 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jnnp.2005.085019 |
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