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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Published in | BMB reports Vol. 48; no. 5; pp. 243 - 248 |
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Main Authors | , |
Format | Journal Article |
Language | English |
Published |
Korea (South)
Korean Society for Biochemistry and Molecular Biology
01.05.2015
생화학분자생물학회 |
Subjects | |
Online Access | Get full text |
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