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Published in 2023 at "Molecular and Cellular Biology"
DOI: 10.1080/10985549.2023.2169563
Abstract: Abstract Spinocerebellar ataxias (SCAs) are autosomal dominant diseases characterized by cerebellar atrophy and ataxia. The SCA subtype SCA34 is caused by specific mutations in the gene ELOVL4, which encodes a fatty acid (FA) elongase that…
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Keywords:
long chain;
ultra long;
acid elongase;
incomplete elongation ... See more keywords