Anle138b ameliorates pathological phenotypes in mouse and cellular models of Huntington’s disease
Authors da Silva Padilha M, Koyuncu S, Chabanis E, Ryazanov S, Leonov A, Vilchez D, Klein R, Giese A, Griesinger C, Dudanova I Journal EMBO Molecular Medicine Citation EMBO Mol Med. 2026 Jun 26. Abstract Huntington’s disease (HD) is a hereditary movement disorder caused by a CAG repeat expansion in


