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Catecholamine exocytosis is diminished in R6/2 Huntington’s disease model mice

✍ Scribed by Michael A. Johnson; Melissa Villanueva; Christy L. Haynes; Andrew T. Seipel; Leah A. Buhler; R. Mark Wightman


Book ID
111180446
Publisher
John Wiley and Sons
Year
2007
Tongue
English
Weight
261 KB
Volume
103
Category
Article
ISSN
0022-3042

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## Background Huntington's disease (HD) is a hereditary neurodegenerative disorder caused by a CAG repeat expansion in the __HD__ gene. The huntingtin protein expressed from __HD__ has an unknown function but is suggested to interact with proteins involved in the cell division machinery. The R6/2 t