LRRK2 in Parkinson's disease and dementia with Lewy bodies

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...

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Bibliografiska uppgifter
Huvudupphovsmän: Zhu Xiongwei, Babar Asim, Siedlak Sandra L, Yang Qiwei, Ito Genta, Iwatsubo Takeshi, Smith Mark A, Perry George, Chen Shu G
Materialtyp: Artikel
Språk:English
Publicerad: BMC 2006-11-01
Serie:Molecular Neurodegeneration
Länkar:http://www.molecularneurodegeneration.com/content/1/1/17

Internet

http://www.molecularneurodegeneration.com/content/1/1/17

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