SCN2A Mutations and Benign Familial Neonatal-Infantile Seizures: The Phenotypic Spectrum (Q58417051)

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SCN2A Mutations and Benign Familial Neonatal-Infantile Seizures: The Phenotypic Spectrum
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    SCN2A mutations and benign familial neonatal-infantile seizures: the phenotypic spectrum (English)

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