Fronto-striatal circuitry in children at risk for Huntington's disease
Huntington's disease (HD) is an autosomal dominant neurodegenerative disease caused by a mutation involving an expansion of the CAG trinucleotide repeats in the gene encoding for huntingtin (HTT) protein. The discovery of the disease-causing faulty gene (mutant huntingtin; mHTT) has enabled val...
| Main Author: | |
|---|---|
| Other Authors: | |
| Format: | Others |
| Language: | English |
| Published: |
University of Iowa
2016
|
| Subjects: | |
| Online Access: | https://ir.uiowa.edu/etd/3126 https://ir.uiowa.edu/cgi/viewcontent.cgi?article=6470&context=etd |