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Autor:
Mackenzie W. Ferguson, Connor J. Kennedy, Thulani H. Palpagama, Henry J. Waldvogel, Richard L. M. Faull, Andrea Kwakowsky
Publikováno v:
Journal of Central Nervous System Disease, Vol 14 (2022)
Huntington’s disease (HD) is an autosomal neurodegenerative disease that is characterized by an excessive number of CAG trinucleotide repeats within the huntingtin gene ( HTT). HD patients can present with a variety of symptoms including chorea, be
Externí odkaz:
https://doaj.org/article/3ab47fb0ae23401182f6158359918c55
