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Genetic analysis of parkin co-regulated gene (PACRG) in patients with early-onset parkinsonism

✍ Scribed by Hao Deng; Wei-Dong Le; Wen-Jie Xie; Tian-Hong Pan; Xiong Zhang; Joseph Jankovic


Book ID
116767697
Publisher
Elsevier Science
Year
2005
Tongue
English
Weight
57 KB
Volume
382
Category
Article
ISSN
0304-3940

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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