A mutation in leucine-rich repeat kinase 2 is the most common cause of hereditary Parkinson's disease (PD), yet the neural mechanisms and the circuitry potentially involved are poorly understood.
Impaired intracortical transmission in G2019S leucine rich-repeat kinase Parkinson patients
Koch, Giacomo
2017-01-01
Abstract
A mutation in leucine-rich repeat kinase 2 is the most common cause of hereditary Parkinson's disease (PD), yet the neural mechanisms and the circuitry potentially involved are poorly understood.File in questo prodotto:
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