Back to search

Article

Structural and functional alterations associated with the LRRK2 G2019S mutation revealed in structured human neural networks

2020-05-02

Abstract excerpt

Mutations in the LRRK2 gene have been widely linked to Parkinson’s disease. The G2019S variant has been shown to contribute uniquely to both familial and sporadic forms of the disease. LRRK2-related mutations have been extensively studied, yet the wide variety of cellular and network events directly or indirectly related to these mutations remain poorly understood. In this study, we structured multi-nodal human ne...

Topics

Open a Topic to create a Post that cites this publication.

Identifiers and source

Literature Corpus work
812f6330-e959-530b-b5e9-83865d18c45d
DOI
10.1101/2020.05.02.073726
Open publication

Related research

Semantic proximity does not establish scientific evidence.

Click a neighbor to travelStep 1 · 12 closest
Interactive article relationship graphSelect a related publication card to move it into the centre and load its closest explainable connections. Solid lines are source-backed structured connections. Dashed lines are semantic discovery signals and are not scientific evidence.
Structural and functional alterations associated with the LRRK2 G2019S mutation revealed in structured human neural networksDOI 10.1101/2020.05.02.073726
Select a neighboring publication to make it the new centre.