Movement Disorder Genomic Study

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Brief description of study

With the present study we aim to perform integrated genomic analysis and study on subject-specific cellular models in order to identify genetic causes of rare or undiagnosed movement disorders. This study will allow to further assess undiagnosed cases and offer the possibility of offering molecular diagnoses to subjects still waiting for a better definition of their conditions.

Clinical Study Identifier: s21-00207

Principal Investigator: Giulietta Maria Riboldi.

Other Investigators: Un Kang, Steven J. Frucht.

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