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<http://identifiers.org/pubmed/19710327> <http://purl.org/dc/terms/title> "A functional null mutation of SCN1B in a patient with Dravet syndrome." <http://purl.org/np/RALOyTVAjZ9P-ltK_50RRd3l7BlrQdzpcgYQUJqyfWYoA#provenance> .
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