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A. Iscan

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Open access Jul 2026

Molecular Analysis of SCN1A Gene Variants Associated with Dravet Syndrome: Implications for Diagnosis and Management.

SCN1A-confirmed DS is associated with substantial seizure burden and neurodevelopmental morbidity, and delayed molecular diagnosis may lead to inappropriate treatment exposure and seizure worsening.

Esma Şengenç, Şeyma Sönmez Şahin, A. Iscan et al. · 0 citations