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2011•Brain and DevelopmentRequires access

On the likelihood of SCN1A microdeletions or duplications in Dravet syndrome with missense mutation

Xiu‐Yu Shi, Jiwen Wang, Hirokazu Kurahashi, Atsushi Ishii, Norimichi Higurashi, Sunao Kaneko, Shinichi Hirose

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Key concepts: Dravet syndrome, Missense mutation, Genetics, Mutation, Medicine, Gene, Biology, Epilepsy

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On the likelihood of SCN1A microdeletions or duplications in Dravet syndrome with missense mutation — Research Paper | ScholarLens