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Abstract
Parkinson disease is a common neurological condition associated with increased morbidity and reduced survival.1-3 The origin of Parkinson disease remains largely elusive, but genetic factors may be important.4,5 One of the most promising leads in the genetics of Parkinson disease is the potential role of the α-synuclein (SNCA) gene. Linkage studies have revealed several SNCA mutations that cause Parkinson disease, likely via amino-acid substitutions and configurational changes in the encoded protein.6-8 α-Synuclein locus multiplication also causes Parkinson disease, likely via gene overexpression.9-13