Altered intrinsic brain functional connectivity in drug-naïve Parkinson’s disease patients with LRRK2 mutations
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DOI: 10.1016/j.neulet.2018.03.038
Abstract: BACKGROUND Leucine-rich repeat kinase 2 (LRRK2) has been recently identified as a causative gene of Parkinson's disease (PD), and the LRRK2 R1628P and G2385R mutations are common in ethnic Han-Chinese PD patients. However, the pathogenic… read more here.
Keywords: patients lrrk2; lrrk2 mutations; drug; han chinese ... See more keywords