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: | , , , , , , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
BMC
2006-11-01
|
Series: | Molecular Neurodegeneration |
Online Access: | http://www.molecularneurodegeneration.com/content/1/1/17 |