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β-Glucocerebrosidase gene mutations in two cohorts of Greek patients with sporadic Parkinson's disease

✍ Scribed by Marina Moraitou; Georgios Hadjigeorgiou; Ioannis Monopolis; Efthimios Dardiotis; Maria Bozi; Demitris Vassilatis; Lluisa Vilageliu; Daniel Grinberg; Georgia Xiromerisiou; Leonidas Stefanis; Helen Michelakakis

Book ID
116989377
Publisher
Elsevier Science
Year
2011
Tongue
English
Weight
163 KB
Volume
104
Category
Article
ISSN
1096-7192

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## Abstract Mutations in the leucine‐rich repeat kinase 2 (__LRRK2__) gene have been shown to cause autosomal dominant and sporadic Parkinson's disease (PD). We report here the frequency of a common heterozygous mutation, 2877510G>A, which produces a glycine‐to‐serine amino acid substitution at cod