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    P607: Identification of pathogenic genetic variants using whole genome sequencing in patients with epilepsy

    P607: Identification of pathogenic genetic variants using whole genome sequencing in patients with epilepsy by Oleksandr Olifir, Claudia Moreau, Maxime Cadieux-Dion, Berge Minassian, Patrick Cossette, Simon Girard

    Published 2024-01-01
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