Title : A role of mitochondrial complex II defects in genetic models of Huntington's disease expressing N-terminal fragments of mutant huntingtin.

Pub. Date : 2013 Oct 1

PMID : 23720495






2 Functional Relationships(s)
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Compound Name
Protein Name
Organism
1 Huntington"s disease (HD) is a neurodegenerative disorder caused by an abnormal expansion of a CAG repeat encoding a polyglutamine tract in the huntingtin (Htt) protein. polyglutamine huntingtin Rattus norvegicus
2 Huntington"s disease (HD) is a neurodegenerative disorder caused by an abnormal expansion of a CAG repeat encoding a polyglutamine tract in the huntingtin (Htt) protein. polyglutamine huntingtin Rattus norvegicus