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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Main Authors: Williams‐Gray, C H, Goris, A, Foltynie, T, Brown, J, Maranian, M, Walton, A, Compston, D A S, Sawcer, S J, Barker, R A
格式: Artigo
語言:Inglês
出版: BMJ Group 2006
主題:
Short Report
在線閱讀: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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