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: Fahr’s disease due to a novel SLC20A2 gene mutation in a Canadian patient: Early Neurocognitive, Structural and Metabolic changes (P2.175)

Researchers

Presenter

  • Leila Sellami

Principal Investigators

  • Louis Verret

  • Stphane Poulin

  • Robert Laforce

Medical Centers

  • 2Psychiatry, Université Laval, Clinique de mémoire, CHU de Québec - Hôpital Enfant-Jésus Quebec QC Canada

  • 2Psychiatry, Université Laval, Clinique de mémoire, CHU de Québec - Hôpital Enfant-Jésus Quebec QC Canada

Locations

  • Canada

Companies

  • N/A

Study Components

Therapeutic Area

  • N/A

Disease

  • N/A

Biomarkers

  • N/A

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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