G2385R and I2020T Mutations Increase LRRK2 GTPase Activity

The LRRK2 mutation is a major causal mutation in familial Parkinson's disease. Although LRRK2 contains functional GTPase and kinase domains and their activities are altered by pathogenic mutations, most studies focused on LRRK2 kinase activity because the most prevalent mutant, G2019S, enhances...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Argitaratua izan da:Biomed Res Int
Egile Nagusiak: Ho, Dong Hwan, Jang, Jihoon, Joe, Eun-hye, Son, Ilhong, Seo, Hyemyung, Seol, Wongi
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: Hindawi Publishing Corporation 2016
Gaiak:
Research Article
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC4897664/
https://ncbi.nlm.nih.gov/pubmed/27314038
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2016/7917128
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