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Published in 2023 at "Biomolecules"
DOI: 10.3390/biom13050788
Abstract: Spinocerebellar ataxia type 1 (SCA1) is an autosomal dominant neurodegenerative disorder that affects one or two individuals per 100,000. The disease is caused by an extended CAG repeat in exon 8 of the ATXN1 gene…
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Keywords:
therapeutic strategies;
sca1;
ataxia type;
strategies spinocerebellar ... See more keywords