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LRRK2: function and dysfunction

28 - 30 March 2012, London, United Kingdom


Introduction
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.
Venue
Royal Holloway, University of London, UK

Royal Holloway, University of London, UK, London, United Kingdom

Organised by
The Biochemical Society
Contact information
Miss Beth Faircliffe
The Biochemical Society, Charles Darwin House, London, WC1N 2JU, United Kingdom
Contact us by email

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