The G2019S LRRK2 Mutation is Rare in Korean Patients with Parkinson's Disease and Multiple System Atrophy

BACKGROUND AND PURPOSE: The LRRK2 (PARK8; OMIM607060) substitution was recently identified as a causative mutation for Parkinson's disease (PD). The pathologic heterogeneity of LRRK2-positive patients suggests that mutation of the LRRK2 gene is associated with the pathogenesis of PD and Parkins...

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Detalles Bibliográficos
Autores principales: Cho, Jin-Whan, Kim, Sung-Yeon, Park, Sung-Sup, Jeon, Beom S.
Formato: Texto
Lenguaje:English
Publicado: Korean Neurological Association 2009
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2686897/
https://www.ncbi.nlm.nih.gov/pubmed/19513331
http://dx.doi.org/10.3988/jcn.2009.5.1.29

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2686897/
https://www.ncbi.nlm.nih.gov/pubmed/19513331
http://dx.doi.org/10.3988/jcn.2009.5.1.29

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