Author Correction: Epilepsy and neuropsychiatric comorbidities in mice carrying a recurrent Dravet syndrome SCN1A missense mutation

Author Correction: Epilepsy and neuropsychiatric comorbidities in mice carrying a recurrent Dravet syndrome SCN1A missense mutation

An amendment to this paper has been published and can be accessed via a link at the top of the paper.

Bibliographic Details
Main Authors:	Ana Ricobaraza, Lucia Mora-Jimenez, Elena Puerta, Rocio Sanchez-Carpintero, Ana Mingorance, Julio Artieda, Maria Jesus Nicolas, Guillermo Besne, Maria Bunuales, Manuela Gonzalez-Aparicio, Noemi Sola-Sevilla, Miguel Valencia, Ruben Hernandez-Alcoceba
Format:	Article
Language:	English
Published:	Nature Publishing Group 2021-04-01
Series:	Scientific Reports
Online Access:	https://doi.org/10.1038/s41598-021-87092-3

Similar Items

Transfer of SCN1A to the brain of adolescent mouse model of Dravet syndrome improves epileptic, motor, and behavioral manifestations
by: Lucia Mora-Jimenez, et al.
Published: (2021-09-01)

Multimodal Analysis of SCN1A Missense Variants Improves Interpretation of Clinically Relevant Variants in Dravet Syndrome
by: Marina C. Gonsales, et al.
Published: (2019-03-01)

Life-span characterization of epilepsy and comorbidities in Dravet syndrome mice carrying a targeted deletion of exon 1 of the Scn1a gene
by: Augusto, J., et al.
Published: (2022)

Study on the effects of Scn1a mutation (Dravet syndrome) in neurogenesis
by: Jui-Hong Hsu, et al.
Published: (2015)

Alterations of the Hippocampal Neurogenic Niche in a Mouse Model of Dravet Syndrome
by: Soraya Martín-Suárez, et al.
Published: (2020-07-01)

Dravet Syndrome in Lebanon: First Report on Cases with SCN1A Mutations
by: Saada Alame, et al.
Published: (2019-01-01)

Identification of SCN1A and PCDH19 mutations in Chinese children with Dravet syndrome.
by: Anna Ka-Yee Kwong, et al.
Published: (2012-01-01)

Proteomic signature of the Dravet syndrome in the genetic Scn1a-A1783V mouse model
by: Nina Miljanovic, et al.
Published: (2021-09-01)

Generation of three human induced pluripotent stem cell (iPSC) lines from three patients with Dravet syndrome carrying distinct SCN1A gene mutations
by: Jens Schuster, et al.
Published: (2019-08-01)

The dose makes the poison-Novel insights into Dravet syndrome and SCN1A regulation through nonproductive splicing.
by: Ingo Helbig, et al.
Published: (2021-01-01)

Understanding the Potential Role of Sirtuin 2 on Aging: Consequences of SIRT2.3 Overexpression in Senescence
by: Noemi Sola-Sevilla, et al.
Published: (2021-03-01)

POGZ de novo missense variants in neuropsychiatric disorders
by: Wenjing Zhao, et al.
Published: (2019-09-01)

Preclinical Animal Models for Dravet Syndrome: Seizure Phenotypes, Comorbidities and Drug Screening
by: Aliesha Griffin, et al.
Published: (2018-06-01)

Establishment of a human induced stem cell line (FUi002-A) from Dravet syndrome patient carrying heterozygous R1525X mutation in SCN1A gene
by: Yasuyoshi Tanaka, et al.
Published: (2018-08-01)

A role of SCN9A in human epilepsies, as a cause of febrile seizures and as a potential modifier of Dravet syndrome.
by: Nanda A Singh, et al.
Published: (2009-09-01)

Inhibitory synaptic transmission is impaired at higher extracellular Ca2+ concentrations in Scn1a +/− mouse model of Dravet syndrome
by: Kouya Uchino, et al.
Published: (2021-05-01)

Dravet syndrome
by: Incorpora Gemma
Published: (2009-09-01)

Kardialer Phänotyp und SUDEP durch Knockout des Nav1.1 Kanalgens (SCN1A) in einem Dravet-Mausmodell
by: Kaiser, Markus Leonhard
Published: (2018)

The Heat Sensing Trpv1 Receptor Is Not a Viable Anticonvulsant Drug Target in the Scn1a+/− Mouse Model of Dravet Syndrome
by: Vaishali Satpute Janve, et al.
Published: (2021-05-01)

In vivo, in vitro and in silico correlations of four de novo SCN1A missense mutations.
by: Andreea Nissenkorn, et al.
Published: (2019-01-01)

Scn1a missense mutation causes limbic hyperexcitability and vulnerability to experimental febrile seizures
by: Yukihiro Ohno, et al.
Published: (2011-02-01)

Phenotypes of Dravet Syndrome
by: Rebecca Garcia-Sosa, et al.
Published: (2016-08-01)

Vaccinations and Dravet Syndrome
by: Christian M. Korff
Published: (2015-12-01)

Neuropsychiatric comorbidity in obesity: role of inflammatory processes
by: Nathalie eCastanon, et al.
Published: (2014-05-01)

Development of screening batteries for neuropsychiatric comorbidity in elderly
by: Yaroslav Winter, et al.
Published: (2013-12-01)

Functional and structural deficits of the dentate gyrus network coincide with emerging spontaneous seizures in an Scn1a mutant Dravet Syndrome model during development
by: Ming-Shian Tsai, et al.
Published: (2015-05-01)

Association of small-fiber polyneuropathy with three previously unassociated rare missense SCN9A variants
by: Mary A. Kelley, et al.
Published: (2020-01-01)

Protein structure aids predicting functional perturbation of missense variants in SCN5A and KCNQ1
by: Brett M. Kroncke, et al.
Published: (2019-01-01)

Comorbid neuropsychiatric and autonomic features in REM sleep behavior disorder
by: Daniel A. Barone, et al.
Published: (2020-01-01)

WHAT IS NEW IN DRAVET SYNDROME?
by: Lucia M. Sur, et al.
Published: (2021-06-01)

Crouch Gait in Dravet Syndrome
by: Laura Black, et al.
Published: (2016-11-01)

Acute Encephalopathy with Dravet Syndrome
by: J Gordon Millichap
Published: (2012-02-01)

ELECTROENCEPHALOGRAPHIC CHANGES WITH DRAVET SYNDROME
by: K. Yu. Mukhin, et al.
Published: (2015-04-01)

Prevalence of SCN1A-related dravet syndrome among children reported with seizures following vaccination: a population-based ten-year cohort study.
by: Nienke E Verbeek, et al.
Published: (2013-01-01)

Rare variants of small effect size in neuronal excitability genes influence clinical outcome in Japanese cases of SCN1A truncation-positive Dravet syndrome.
by: Michael F Hammer, et al.
Published: (2017-01-01)

Rare variants of small effect size in neuronal excitability genes influence clinical outcome in Japanese cases of SCN1A truncation-positive Dravet syndrome
by: Hammer, Michael F., et al.
Published: (2017)

CRISPR/dCas9-based Scn1a gene activation in inhibitory neurons ameliorates epileptic and behavioral phenotypes of Dravet syndrome model mice
by: Tetsushi Yamagata, et al.
Published: (2020-07-01)

SCN2A channelopathies in the autism spectrum of neuropsychiatric disorders: a role for pluripotent stem cells?
by: Karina A. Kruth, et al.
Published: (2020-04-01)

A Missense Variant in <i>SCN8A</i> in Alpine Dachsbracke Dogs Affected by Spinocerebellar Ataxia
by: Anna Letko, et al.
Published: (2019-05-01)

Slitrk missense mutations associated with neuropsychiatric disorders distinctively impair Slitrk trafficking and synapse formation
by: Hyeyeon Kang, et al.
Published: (2016-10-01)

Cannot write session to /tmp/vufind_sessions/sess_dq6ssmuhjkagd51gmu86mj83sj