Modelling and analysis of LRRK2 mutations in iPSC-derived dopaminergic neurons and astrocytes

Parkinson's disease (PD) is a common neurodegenerative disorder, characterised by preferential loss of ventral midbrain dopaminergic (vmDA) neurons in the substantia nigra pars compacta (SNc). The majority of PD cases have unknown aetiology; however, between 5-10% arise due to known genetic mut...

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Bibliographic Details
Main Author: Booth, Heather D. E.
Other Authors: Wade-Martins, Richard
Published: University of Oxford 2017
Online Access:https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.740946