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Autor:
Maria Daniela Cirnaru, Antonella eMarte, Elisa eBelluzzi, Isabella eRusso, Martina eGabrielli, Francesco eLongo, Ludovico eArcuri, Luca eMurru, Luigi eBubacco, Michela eMatteoli, Ernesto eFedele, Carlo eSala, Maria ePassafaro, Michele eMorari, Elisa eGreggio, Franco eOnofri, Giovanni ePiccoli
Publikováno v:
Frontiers in Molecular Neuroscience, Vol 7 (2014)
Mutations in Leucine-rich repeat kinase 2 gene (LRRK2) are associated with familial and sporadic Parkinson’s disease (PD). LRRK2 is a complex protein that consists of multiple domains executing several functions, including GTP hydrolysis, kinase ac
Externí odkaz:
https://doaj.org/article/fc81bc2378104db58a48beabcd795f47
