A series of N-terminal epitope tagged <it>Hdh</it> knock-in alleles expressing normal and mutant huntingtin: their application to understanding the effect of increasing the length of normal huntingtin’s polyglutamine stretch on CAG140 mouse model pathogenesis
<p>Abstract</p> <p>Background</p> <p>Huntington’s disease (HD) is an autosomal dominant neurodegenerative disease that is caused by the expansion of a polyglutamine (polyQ) stretch within Huntingtin (htt), the protein product of the HD gene. Although studies in vitro ha...
Main Authors: | , , , , |
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Format: | Article |
Language: | English |
Published: |
BMC
2012-08-01
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Series: | Molecular Brain |
Subjects: | |
Online Access: | http://www.molecularbrain.com/content/5/1/28 |