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A functional polymorphism in the parkin gene promoter affects the age of onset of Parkinson's disease

✍ Scribed by Greg Sutherland; George Mellick; Carolyn Sue; Daniel K.Y. Chan; Dominic Rowe; Peter Silburn; Glenda Halliday


Book ID
116769306
Publisher
Elsevier Science
Year
2007
Tongue
English
Weight
146 KB
Volume
414
Category
Article
ISSN
0304-3940

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Deletion of the parkin and PACRG gene pr
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## Communicated by Christine Van Broeckhoven Autosomal recessive mutations in the parkin gene (PARK2) have been identified as a common cause of familial and also sporadic, early-onset parkinsonism (EOPD): point mutations, exonic deletions, and duplications or triplications have been described. Her