Behavioral characterization of P311 knockout mice

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Correction: Behavioral and Electrophysiological Characterization of Dyt1 Heterozygous Knockout Mice

The following information is missing from the Funding section: This study was supported by the Bachmann-Strauss Dystonia and Parkinson Foundation, Inc. The complete, correct funding information is as follows: This work was supported by Tyler’s Hope for a Dystonia Cure, Inc., Dystonia Medical Research Foundation, Bachmann-Strauss Dystonia and Parkinson Foundation, Inc., National Institutes of He...

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Behavioral and Electrophysiological Characterization of Dyt1 Heterozygous Knockout Mice

DYT1 dystonia is an inherited movement disorder caused by mutations in DYT1 (TOR1A), which codes for torsinA. Most of the patients have a trinucleotide deletion (ΔGAG) corresponding to a glutamic acid in the C-terminal region (torsinA(ΔE)). Dyt1 ΔGAG heterozygous knock-in (KI) mice, which mimic ΔGAG mutation in the endogenous gene, exhibit motor deficits and deceased frequency of spontaneous ex...

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ژورنال

عنوان ژورنال: Genes, Brain and Behavior

سال: 2008

ISSN: 1601-1848,1601-183X

DOI: 10.1111/j.1601-183x.2008.00420.x