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

doi:10.1016/j.seizure.2020.04.004

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 journal › Comment/debate › peer-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 language	English (US)
Pages (from-to)	281
Number of pages	1
Journal	Seizure
Volume	80
DOIs	https://doi.org/10.1016/j.seizure.2020.04.004
State	Published - Aug 2020

ASJC Scopus subject areas

Neurology
Clinical Neurology

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Gertler, T. S., Calhoun, J., & Laux, L. (2020). 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)). Seizure, 80, 281. https://doi.org/10.1016/j.seizure.2020.04.004

Gertler, Tracy S. ; Calhoun, Jeffrey ; Laux, Linda. / 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)). In: Seizure. 2020 ; Vol. 80. pp. 281.

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title = "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))",

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.",

author = "Gertler, {Tracy S.} and Jeffrey Calhoun and Linda Laux",

note = "Publisher Copyright: {\textcopyright} 2020 British Epilepsy Association",

year = "2020",

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doi = "10.1016/j.seizure.2020.04.004",

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Gertler, TS , Calhoun, J & Laux, L 2020, '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))', Seizure, vol. 80, pp. 281. https://doi.org/10.1016/j.seizure.2020.04.004

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)). / Gertler, Tracy S.; Calhoun, Jeffrey ; Laux, Linda.
In: Seizure, Vol. 80, 08.2020, p. 281.

Research output: Contribution to journal › Comment/debate › peer-review

TY - JOUR

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AU - Gertler, Tracy S.

AU - Calhoun, Jeffrey

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AB - 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.

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Gertler TS , Calhoun J , Laux L. 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)). Seizure. 2020 Aug;80:281. doi: 10.1016/j.seizure.2020.04.004

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))

Abstract

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