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: CAPN1: novel mutations expanding the phenotype of hereditary spastic paraparesis. (P6.039)

Researchers

Presenter

  • Aakash Shetty

Principal Investigators

  • Setareh Ashtiani

  • Ziv Gan-Or

  • Bart Van de Warrenburg

  • Tessa Wassenberg

  • Guy Rouleau

  • Oksana Suchowersky

Medical Centers

  • 1Medicine (Neurology), University of Alberta Edmonton AB Canada

  • Department of Neurology and Neurosurgery, McGill University, Montreal, Canada

  • Experimential Rheumatology, Radboud university medical center, Nijmegen, Netherlands

Locations

  • Canada

  • Netherlands

Companies

  • N/A

Study Components

Therapeutic Area

  • Central Nervous System (CNS)

  • Genetic Disorder

Disease

  • N/A

Biomarkers

  • Calpain 1

Drug/Treatment

  • N/A

Outcome

  • N/A

Study Design

  • N/A

Phase

  • NA

Study Id's

  • N/A

Sponsors

  • N/A

Result

  • N/A

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