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Genotype, Disease Onset, And Neurocognitive Phenotype Of Sanfilippo Syndrome Type A

โœ Scribed by Chester B. Whitley; Renee Cooksley; Brenda Diethelm-Okita; Kathleen Delaney; Patrick Haslett; Charles Richard; Elsa Shapiro


Book ID
116989638
Publisher
Elsevier Science
Year
2012
Tongue
English
Weight
54 KB
Volume
105
Category
Article
ISSN
1096-7192

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## Abstract Early onset Parkinson's disease (EOPD) has been associated with mutations in the __Parkin__, __DJโ€1, PINK1, LRRK2,__ and __SNCA__ genes. The aim of this study is to assess the contribution of these genes in a Dutch EOPD cohort and the phenotypic characteristics of the mutation carriers.