Mouse models for Huntington’s disease research are invaluable tools for studying the genetic and pathological aspects of this neurodegenerative disorder. These models replicate the mutant huntingtin gene, leading to motor dysfunction, cognitive decline, and neuronal loss. By using these models, researchers can investigate disease mechanisms, test therapeutic interventions, and explore potential biomarkers. This approach accelerates the development of treatments and deepens our understanding of Huntington’s disease progression.