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Published in 2022 at "PLOS ONE"
DOI: 10.1371/journal.pone.0278130
Abstract: Huntington’s disease is an autosomal dominant heritable disorder caused by an expanded CAG trinucleotide repeat at the N-terminus of the Huntingtin (HTT) gene. Lowering the levels of soluble mutant HTT protein prior to aggregation through…
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Keywords:
pa28 activation;
aggregation;
reduction pa28;
mutant htt ... See more keywords