J. Garrels

Genetic heterogeneity in ten families with myoclonus-dystonia

L. Ozelius, V. Kostic, C. Klein, 2004, Journal of Neurology, Neurosurgery & Psychiatry.

Role of parkin mutations in 111 community‐based patients with early‐onset parkinsonism

Christine Klein, Katja Hedrich, X. Breakefield, 2002, Annals of neurology.

Distribution, type, and origin of Parkin mutations: Review and case studies

K. Marder, A. Lang, Juliette M. Harris, 2004, Movement disorders : official journal of the Movement Disorder Society.

Evidence that paternal expression of the epsilon-sarcoglycan gene accounts for reduced penetrance in myoclonus-dystonia.

W. Reik, M. Nitschke, P. Pramstaller, 2002, American journal of human genetics.

Myoclonus–dystonia: Detection of novel, recurrent, and de novo SGCE mutations

Karl E. Wiegers, B. Landwehrmeyer, J. Koelman, 2004, Neurology.

Hereditary myoclonus–dystonia associated with epilepsy

E. Foncke, J. Koelman, M. Tijssen, 2003, Neurology.

Phenotypic features of myoclonus-dystonia in three kindreds

M. Brin, S. Bressman, M. Tijssen, 2002, Neurology.

A major locus for myoclonus-dystonia maps to chromosome 7q in eight families.

M. Brin, A. Lang, X. Breakefield, 2000, American journal of human genetics.

Mutations in DYT1

R. Lencer, X. Breakefield, K. Witt, 2004, Neurology.

Association studies of Parkinson's disease and parkin polymorphisms

P. Pramstaller, P. Vieregge, L. Ozelius, 2000, Annals of neurology.