Cargando…

Correction to: Dravet syndrome-associated mutations in GABRA1, GABRB2 and GABRG2 define the genetic landscape of defects of GABA(A) receptors

Detalles Bibliográficos
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Oxford University Press 2022
Materias:	Correction
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9234060/ https://www.ncbi.nlm.nih.gov/pubmed/35770130 http://dx.doi.org/10.1093/braincomms/fcac156

Ejemplares similares

Dravet syndrome-associated mutations in GABRA1, GABRB2 and GABRG2 define the genetic landscape of defects of GABA(A) receptors
por: Hernandez, Ciria C, et al.
Publicado: (2021)

Molecular and clinical descriptions of patients with GABA(A) receptor gene variants ( GABRA1, GABRB2, GABRB3, GABRG2 ): A cohort study, review of literature, and genotype–phenotype correlation
por: Maillard, Pierre‐Yves, et al.
Publicado: (2022)

The Effects of Gene Variations of GABRA2, GABRB1, GABRG2, GAD1 and SLC1A3 on Patients with Propofol During Anesthesia Induction
por: Zhang, Lingyi, et al.
Publicado: (2021)

GABRA1 and GABRB2 Polymorphisms are Associated with Propofol Susceptibility
por: Zeng, Youjie, et al.
Publicado: (2022)

Paradoxical worsening of seizure activity with pregabalin in an adult with isodicentric 15 (IDIC-15) syndrome involving duplications of the GABRB3, GABRA5 and GABRG3 genes
por: Di Rocco, Alessandro, et al.
Publicado: (2013)

An association study in the Taiwan Biobank elicits the GABAA receptor genes GABRB3, GABRA5, and GABRG3 as candidate loci for sleep duration in the Taiwanese population
por: Hou, Sheue-Jane, et al.
Publicado: (2021)

Gabra2 is a genetic modifier of Dravet syndrome in mice
por: Hawkins, Nicole A., et al.
Publicado: (2021)

Analysis of GABRG2 C588T polymorphism in genetic epilepsy and evaluation of GABRG2 in drug treatment
por: Wang, Shitao, et al.
Publicado: (2021)

A novel GABRB3 variant in Dravet syndrome: Case report and literature review
por: Pavone, Piero, et al.
Publicado: (2020)

A standardized polyherbal preparation POL-6 diminishes alcohol withdrawal anxiety by regulating Gabra1, Gabra2, Gabra3, Gabra4, Gabra5 gene expression of GABA(A) receptor signaling pathway in rats
por: Sharma, Lalit, et al.
Publicado: (2021)

Role of gabra2, GABA(A) receptor alpha-2 subunit, in CNS development
por: Gonzalez-Nunez, Veronica
Publicado: (2015)

Novel GABRG2 mutations cause familial febrile seizures
por: Boillot, Morgane, et al.
Publicado: (2015)

Correction to: Pathophysiology of and therapeutic options for a GABRA1 variant linked to epileptic encephalopathy
por: Bai, Yun-Fei, et al.
Publicado: (2020)

GABRG2 Variants Associated with Febrile Seizures
por: Hernandez, Ciria C., et al.
Publicado: (2023)

Novel SCN1A and GABRA1 Gene Mutations With Diverse Phenotypic Features and the Question on the Existence of a Broader Spectrum of Dravet Syndrome
por: Gontika, Maria P., et al.
Publicado: (2017)

The GABA(A) receptor α2 subunit gene (GABRA2) is associated with alcohol-related behavior
por: Švob Štrac, Dubravka, et al.
Publicado: (2012)

GABA(A) Receptor Coupling Junction and Pore GABRB3 Mutations are Linked to Early-Onset Epileptic Encephalopathy
por: Hernandez, Ciria C., et al.
Publicado: (2017)

Correction to: Fenfluramine: A Review in Dravet and Lennox-Gastaut Syndromes
por: Frampton, James E.
Publicado: (2023)

Correction: Sporadic Infantile Epileptic Encephalopathy Caused by Mutations in PCDH19 Resembles Dravet Syndrome but Mainly Affects Females
por: Depienne, Christel, et al.
Publicado: (2009)

Phenotypic Spectrum and Prognosis of Epilepsy Patients With GABRG2 Variants
por: Yang, Ying, et al.
Publicado: (2022)

A novel de novo variant of GABRA1 causes increased sensitivity for GABA in vitro
por: Steudle, Friederike, et al.
Publicado: (2020)

Abnormal expression of GABA(A) receptor subunits and hypomotility upon loss of gabra1 in zebrafish
por: Reyes-Nava, Nayeli G., et al.
Publicado: (2020)

Personalized medicine: Vinpocetine to reverse effects of GABRB3 mutation
por: Billakota, Santoshi, et al.
Publicado: (2019)

Phenotype Expression Variability in Children with GABRB3 Heterozygous Mutations
por: Khair, Abdulhafeez M., et al.
Publicado: (2021)

No Gain, Less Pain: GABRB3 Mutations in Epileptic Encephalopathy
por: Gallagher, Martin J.
Publicado: (2022)

A de novo missense mutation of GABRB2 causes early myoclonic encephalopathy
por: Ishii, Atsushi, et al.
Publicado: (2017)

Human GABRG2 generalized epilepsy: Increased somatosensory and striatothalamic connectivity
por: Pedersen, Mangor, et al.
Publicado: (2019)

The Human Epilepsy Mutation GABRG2(Q390X) Causes Chronic Subunit Accumulation and Neurodegeneration
por: Kang, Jing-Qiong, et al.
Publicado: (2015)

Genetic variation in GABRA2 moderates peer influence on externalizing behavior in adolescents
por: Villafuerte, Sandra, et al.
Publicado: (2014)

Gabra2 is a genetic modifier of Scn8a encephalopathy in the mouse*
por: Yu, Wenxi, et al.
Publicado: (2020)

Social Cognitive Role of Schizophrenia Candidate Gene GABRB2
por: Tsang, Shui Ying, et al.
Publicado: (2013)

GABRB2 Haplotype Association with Heroin Dependence in Chinese Population
por: Kim, Yung Su, et al.
Publicado: (2015)

Author Correction: Epilepsy and neuropsychiatric comorbidities in mice carrying a recurrent Dravet syndrome SCN1A missense mutation
por: Ricobaraza, Ana, et al.
Publicado: (2021)

Altered Channel Conductance States and Gating of GABA(A) Receptors by a Pore Mutation Linked to Dravet Syndrome
por: Hernandez, Ciria C., et al.
Publicado: (2017)

A Recombination Hotspot in a Schizophrenia-Associated Region of GABRB2
por: Ng, Siu-Kin, et al.
Publicado: (2010)

FRMD7 Mutations Disrupt the Interaction with GABRA2 and May Result in Infantile Nystagmus Syndrome
por: Jiang, Lei, et al.
Publicado: (2020)

Mutations in GABRG2 receptor gene are not a major factor in the pathogenesis of mesial temporal lobe epilepsy in Indian population
por: Dixit, Aparna Banerjee, et al.
Publicado: (2016)

Correction: Defining the Transcriptional and Cellular Landscape of Type 1 Diabetes in the NOD Mouse
por: Carrero, Javier A., et al.
Publicado: (2014)

Neocortex- and hippocampus-specific deletion of Gabrg2 causes temperature-dependent seizures in mice
por: Li, Xinxiao, et al.
Publicado: (2021)

Genetic analysis of GABRB3 as a candidate gene of autism spectrum disorders
por: Chen, Chia-Hsiang, et al.
Publicado: (2014)

Cannot write session to /tmp/vufind_sessions/sess_6ddp3105qrpc91ofp7feos21me