Subtle microstructural changes of the striatum in a DYT1 knock-in mouse model of dystonia

The dystonias are comprised of a group of disorders that share common neurological abnormalities of involuntary twisting or repetitive movements and postures. The most common inherited primary dystonia is DYT1 dystonia, which is due to loss of a GAG codon in the TOR1A gene that encodes torsinA. Auto...

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Bibliographic Details

Published in:	Neurobiology of Disease
Main Authors:	Chang-Hyun Song, Douglas Bernhard, Caroline Bolarinwa, Ellen J. Hess, Yoland Smith, H.A. Jinnah
Format:	Article
Language:	English
Published:	Elsevier 2013-06-01
Subjects:	Mouse mutant Anatomy Golgi histochemistry Stereology Striatum Electron microscopy
Online Access:	http://www.sciencedirect.com/science/article/pii/S0969996113000326