The role of monogenic genes in idiopathic Parkinson’s disease

In the past two decades, mutations in multiple genes have been linked to autosomal dominant or recessive forms of monogenic Parkinson’s disease (PD). Collectively, these monogenic (often familial) cases account for less than 5% of all PD, the majority being apparently sporadic cases. More recently,...

Full description

Bibliographic Details
Main Authors: Xylena Reed, Sara Bandrés-Ciga, Cornelis Blauwendraat, Mark R. Cookson
Format: Article
Language:English
Published: Elsevier 2019-04-01
Series:Neurobiology of Disease
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S0969996118306685