2021
DOI: 10.1212/nxg.0000000000000604
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KCNQ2 Encephalopathy Manifesting With Rett-like Features

Abstract: In the Clinical/Scientific Note "KCNQ2 encephalopathy manifesting with Rett-like features: A follow-up into adulthood" by Mastrangelo et al., 1 the first sentence of the fifth paragraph should read, "A next-generation sequencing panel that included 140 genes involved in genetic epilepsies revealed the de novo heterozygous KCNQ2 variant c.629 G > C (p.Arg210Pro), which was not present in the Human Gene Mutation Database

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