Novel proteomic changes in brain mitochondria provide insights into mitochondrial dysfunction in mouse models of Huntington's disease
Author:
Funder
NINDS
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Molecular Medicine
Reference93 articles.
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3. Dysfunctional mitochondrial respiration in the striatum of the Huntington's disease transgenic R6/2 mouse model;Aidt;PLoS Curr,2013
4. No evidence for increased oxidative damage to lipids, proteins, or DNA in Huntington's disease;Alam;J. Neurochem.,2000
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