LRRK2 in Parkinson's disease and dementia with Lewy bodies
<p>Abstract</p> <p>Background</p> <p>Mutations in <it>LRRK2 </it>encoding leucine-rich repeat kinase 2 are thus far the most frequent genetic cause associated with autosomal dominant and idiopathic Parkinson's disease (PD). To examine whether LRRK2 is d...
Main Authors: | Zhu Xiongwei, Babar Asim, Siedlak Sandra L, Yang Qiwei, Ito Genta, Iwatsubo Takeshi, Smith Mark A, Perry George, Chen Shu G |
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Format: | Article |
Language: | English |
Published: |
BMC
2006-11-01
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Series: | Molecular Neurodegeneration |
Online Access: | http://www.molecularneurodegeneration.com/content/1/1/17 |
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