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Autor:
Laura Gantley, Brett W. Stringer, Vanessa M. Conn, Youichirou Ootsuka, Duncan Holds, Mark Slee, Kamelya Aliakbari, Kirsty Kirk, Rebecca J. Ormsby, Stuart T. Webb, Adrienne Hanson, He Lin, Luke A. Selth, Simon J. Conn
Publikováno v:
Cells, Vol 12, Iss 9, p 1337 (2023)
Trinucleotide repeat disorders comprise ~20 severe, inherited, human neuromuscular and neurodegenerative disorders, which result from an abnormal expansion of repetitive sequences in the DNA. The most common of these, Huntington’s disease (HD), res
Externí odkaz:
https://doaj.org/article/44403ff8fe62462eb9bb5985f0998266
