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A mutation in the human neurofilament M gene in Parkinson's disease that suggests a role for the cytoskeleton in neuronal degeneration

✍ Scribed by Christian Lavedan; Stephanie Buchholtz; Robert L. Nussbaum; Roger L. Albin; Mihael H. Polymeropoulos

Book ID
117472405
Publisher
Elsevier Science
Year
2002
Tongue
English
Weight
280 KB
Volume
322
Category
Article
ISSN
0304-3940

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## Abstract Multiple genes have been now identified as causing Parkinson's disease (PD). In 2003, two mutations were identified in exon 1 of the Nurr1 gene in 10 of 107 individuals with familial PD. To date, investigators have only focused on screening for these known mutations of the Nurr1 gene. A