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Article

A two-hit story: Seizures and genetic mutation interaction sets phenotype severity in SCN1A epilepsies

17 Jan 2019

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Share to Epilepsy research and treatment
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 30659983
DOI: 10.1016/j.nbd.2019.01.006

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