Function and dysfunction of leucine-rich repeat kinase 2 (LRRK2): Parkinson's disease and beyond

Mutations in leucine-rich repeat kinase 2 (LRRK2) are the most common cause of familial Parkinson's disease (PD). As such, functions and dysfunctions of LRRK2 in PD have been the subject of extensive investigation. In addition to PD, increasing evidence is suggesting that LRRK2 is associated wi...

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Bibliographic Details
Published inBMB reports Vol. 48; no. 5; pp. 243 - 248
Main Authors Bae, Jae Ryul, Lee, Byoung Dae
Format Journal Article
LanguageEnglish
Published Korea (South) Korean Society for Biochemistry and Molecular Biology 01.05.2015
생화학분자생물학회
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