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.
Titolo: | Impaired intracortical transmission in G2019S leucine rich-repeat kinase Parkinson patients |
Autori: | KOCH, GIACOMO (Corresponding) |
Data di pubblicazione: | 2017 |
Rivista: | |
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. |
Handle: | http://hdl.handle.net/11389/28652 |
Appare nelle tipologie: | 1.1 Articolo in rivista |
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