Article
Polyglutamine domain flexibility mediates the proximity between flanking sequences in huntingtin.
Proceedings of the National Academy of Sciences of the United States of America - 3 Sept 2013
Caron Nicholas Stephane, Desmond Carly Robyn, Xia Jianrun, Truant Ray
Abstract excerpt
Huntington disease (HD) is a neurodegenerative disorder caused by a CAG expansion within the huntingtin gene that encodes a polymorphic glutamine tract at the amino terminus of the huntingtin protein. HD is one of nine polyglutamine expansion diseases. The clinical threshold of polyglutamine expansion for HD is near 37 repeats, but the mechanism of this pathogenic length is poorly understood. Using Förster...
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