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Huntington disease (HD) is an autosomal neurodegenerative disease caused by the excess of CAG trinucleotide repeats in the Huntington gene (HTT). In addition to various symptoms such as chorea, movement disorders, cognitive impairment and psychosis, patients with HD may also experience behavioral and physical changes. Although there is no known cur... Read More»
Tinku Kumar, Girendra Kumar Gautam, Rohit Malik and Amal Kumar
: J Nov Physiother 2024, 14:704
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