A novel heterozygous SETX mutation in a patient presenting with chorea and motor neuron disease

Enrico SaracchiDepartment of Neurology, San Gerardo Hospital, University of Milano-Bicocca, Monza

Marianna CastelliScientific Institute IRCCS E. Medea, Laboratory of Molecular Biology, Bosisio Parini, Lecco

Maria T. BassiScientific Institute IRCCS E. Medea, Laboratory of Molecular Biology, Bosisio Parini, Lecco

Erika BrighinaScientific Institute IRCCS E. Medea, Neuromuscular Unit, Bosisio Parini, Lecco

Diletta CeredaDepartment of Neurology, San Gerardo Hospital, University of Milano-Bicocca, Monza

Laura MarzoratiDepartment of Neurology, San Gerardo Hospital, University of Milano-Bicocca, Monza

Mirko PatassiniNeuroradiology Service, San Gerardo Hospital, Monza, Italy

Ildebrando AppollonioDepartment of Neurology, San Gerardo Hospital, University of Milano-Bicocca, Monza

Carlo FerrareseDepartment of Neurology, San Gerardo Hospital, University of Milano-Bicocca, Monza

Laura BrighinaDepartment of Neurology, San Gerardo Hospital, University of Milano-Bicocca, MonzaCorrespondence[email protected]

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Declaration of interest: The authors report no conflicts of interest. The authors alone are responsible for the content and writing of the paper.

Supplementary material available online at http://informahealthcare.com/doi/abs/10.3109/21678421.2013.865751

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A novel heterozygous SETX mutation in a patient presenting with chorea and motor neuron disease

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