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Autor:
Sara Gutiérrez-Ángel, Elena Katharina Schulz-Trieglaff, Fabian Hosp, Kerstin Voelkl, Ruediger Klein, Matthias Mann, Jakob M. Bader, Irina Dudanova, Sabine Liebscher, Johanna Burgold, Thomas Arzberger
Publikováno v:
Scientific Reports
Scientific reports 9(1), 6634 (2019). doi:10.1038/s41598-019-43024-w
Scientific Reports, Vol 9, Iss 1, Pp 1-13 (2019)
Scientific reports 9(1), 6634 (2019). doi:10.1038/s41598-019-43024-w
Scientific Reports, Vol 9, Iss 1, Pp 1-13 (2019)
Huntington’s disease (HD) is a devastating hereditary movement disorder, characterized by degeneration of neurons in the striatum and cortex. Studies in human patients and mouse HD models suggest that disturbances of neuronal function in the neocor