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One of its most common hereditary forms, spinocerebellar ataxia type 3 (SCA3), stems from a genetic mutation in the ATXN3 gene and progressively damages the cerebellum

Potential Benefits Works through amylin receptors rather than GLP-1, offering an alternative pathway for patients who may not respond optimally to GLP-1 medications alone

A total of n = 14 RD and n = 14 WD mice were used for body composition measurements

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