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Autor:
Simone Rolfes, David A.D. Munro, Ekaterini-Maria Lyras, Eduardo Matute, Koliane Ouk, Christoph Harms, Chotima Böttcher, Josef Priller
Publikováno v:
Neurobiology of Disease, Vol 144, Iss , Pp 105024- (2020)
Huntington's disease (HD) is an incurable neurodegenerative disorder caused by a trinucleotide (CAG) repeat expansion in the huntingtin gene (HTT). The R6/2 transgenic mouse model of HD expresses exon 1 of the human HTT gene with approximately 150 CA
Externí odkaz:
https://doaj.org/article/37ce36bf12ec4689a5cca9af05cd20c5
