Corrigendum to “A single-center, retrospective analysis of genotype–phenotype correlations in children with Dravet syndrome” [Seizure: Eur. J. Epilepsy 75 (2020) 1–6] (Seizure: European Journal of Epilepsy (2020) 75 (1–6), (S1059131119304467), (10.1016/j.seizure.2019.12.009))

Tracy S. Gertler*, Jeffrey Calhoun, Linda Laux

*Corresponding author for this work

Research output: Contribution to journalComment/debatepeer-review

Abstract

The authors regret that several of the SCN1A variants reported in the supplementary table were annotated incorrectly per chart reports, and appreciate the assistance of the HGMD editors in correcting these variants. In the Results section, p.Ala1442Val should be noted as p.Ala1440Val, and p.Phe1761Thrfs*8 should be noted as p.Phe1671Thrfs*8. Appropriate corrections to all other variants are provided in updated supplementary tables (see attachment) verified through sequence alignment to the cDNA RefSeq for transcript variant 1 of SCN1A (NM_001165963.4) and original genetic testing reports wherever possible. The authors would like to apologise for any inconvenience caused.

Original languageEnglish (US)
Pages (from-to)281
Number of pages1
JournalSeizure
Volume80
DOIs
StatePublished - Aug 2020

ASJC Scopus subject areas

  • Neurology
  • Clinical Neurology

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