In Vitro Expansion of CAG, CAA, and Mixed CAG/CAA Repeats
Polyglutamine diseases, including Huntington’s disease and a number of spinocerebellar ataxias, are caused by expanded CAG repeats that are located in translated sequences of individual, functionally-unrelated genes. Only mutant proteins containing polyglutamine expansions have long been thought to...
Main Authors: | , , |
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Format: | Article |
Language: | English |
Published: |
MDPI AG
2015-08-01
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Series: | International Journal of Molecular Sciences |
Subjects: | |
Online Access: | http://www.mdpi.com/1422-0067/16/8/18741 |