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Your search keyword '"Prehl I"' showing total 3 results

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3 results on '"Prehl I"'

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1. Mutations in the sodium channel gene SCN2A cause neonatal epilepsy with late-onset episodic ataxia

2. Comprehensive NGS-Based Diagnostics in over 800 Patients with Epileptic Encephalopathy

3. Comprehensive NGS-Based Diagnostics in More Than 1,000 Patients with Epileptic Disorders

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