LRRK2: function and dysfunction

Venue: Royal Holloway, University of London

Location: London, United Kingdom

Event Date/Time: Mar 28, 2012 End Date/Time: Mar 30, 2012
Registration Date: Mar 27, 2012
Early Registration Date: Feb 27, 2012
Abstract Submission Date: Feb 01, 2012
Paper Submission Date: Feb 01, 2012
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Mutations in the multidomain enzyme LRRK2 are the most common genetic cause of Parkinson’s disease, but despite intensive investigation we still know very little about the normal function of this protein or how mutations lead to disease.