Title : Mitochondrial dysfunction, metabolic deficits, and increased oxidative stress in Huntington's disease.

Pub. Date : 2011 Mar-Apr

PMID : 21539755






1 Functional Relationships(s)
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Protein Name
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1 The underlying molecular genetic defect is an expanded trinucleotide (CAG)n repeat encoding a polyglutamine stretch in the N-terminus of the huntingtin protein. trinucleotide huntingtin Homo sapiens