J. Bonet

Mutations in THAP1/DYT6 reveal that diverse dystonia genes disrupt similar neuronal pathways and functions

R. Blitzer, M. Ehrlich, T. Zwaka, 2018, PLoS genetics.

Abnormalities of motor function, transcription and cerebellar structure in mouse models of THAP1 dystonia.

P. Hof, M. Ehrlich, P. Gonzalez-Alegre, 2015, Human molecular genetics.

Abnormalities of motor function, transcription and cerebellar structure in mouse models of THAP1 dystonia.

P. Hof, M. Ehrlich, P. Gonzalez-Alegre, 2015, Human Molecular Genetics.