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SynthesisNeurogenetics2021

Dravet syndrome and Dravet syndrome-like phenotype: a systematic review of the SCN1A and PCDH19 variants.

Ana Carla Mondek Rampazzo et al.PubMed ↗Publisher ↗

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7 papers cite it

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Full record →Abstract, authors, funding and every citing paper · PMID 33937968