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Autor:
Javier Ojalvo-Pacheco, Sokhna M. S. Yakhine-Diop, José M. Fuentes, Marta Paredes-Barquero, Mireia Niso-Santano
Publikováno v:
Biology, Vol 13, Iss 4, p 238 (2024)
Huntington’s disease (HD) is an autosomal dominant neurodegenerative disease caused by an expansion of the CAG trinucleotide repeat in exon 1 of the huntingtin (HTT) gene. This expansion leads to a polyglutamine (polyQ) tract at the N-terminal end
Externí odkaz:
https://doaj.org/article/48af2c48b8b84bc3844ba079439145bf
