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Kyono K, Hashimoto T, Kikuchi S, Nagai Y, Sakuraba Y
Preclinical studies investigating KD in HD have primarily used transgenic mouse models, such as the R6/2 mice, which express mutant huntingtin and exhibit progressive motor deficits, weight loss, cognitive impairment, and mitochondrial dysfunction, mimicking central functional and metabolic aspects of HD progression [95, 96]
1 Review Taken along with Glucosamine &