Article
Study of cholesterol metabolism in Huntington's disease.
Biochemical and biophysical research communications - 11 Apr 2014
Leoni Valerio, Caccia Claudio
Abstract excerpt
Huntington's disease (HD) is an autosomal dominant neurodegenerative disorder caused by an abnormal expansion of a CAG repeat in the huntingtin gene. Neurodegeneration of striatum and cortex with a severe atrophy at MRI are common findings in HD. The expression of genes involved in the cholesterol biosynthetic pathway such as HMG-CoA reductase and the levels of cholesterol, lanosterol, lathosterol and...
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