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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

Useful links

Organised by

The Biochemical Society

Contact information

Miss Beth Faircliffe
The Biochemical Society, Charles Darwin House, London, WC1N 2JU, United Kingdom
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