Cui-xia Fan
Key Laboratory Of Neurogenetics And Channelopathies Of Guangdong Province And The Ministry Of Education Of China
Guangzhou, 510260, China
Guangzhou, 510260, China
Last Updated: 09/26/2026
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Found 11 publications
Reply: USP25 in genetic generalized epilepsy: a gene under scrutiny.
Journal: Brain : a journal of neurology
Published: August 15, 2025
De novo heterozygous missense variants in ATP11A are associated with refractory focal epilepsy.
Journal: Journal of medical genetics
Published: November 25, 2024
Corrigendum: ATP6V0C is associated with febrile seizures and epilepsy with febrile seizures plus.
Journal: Frontiers in molecular neuroscience
Published: February 14, 2024
Heterozygous variants in USP25 cause genetic generalized epilepsy.
Journal: Brain : a journal of neurology
Published: January 24, 2024
NUS1 Variants Cause Lennox-Gastaut Syndrome Related to Unfolded Protein Reaction Activation.
Journal: Molecular neurobiology
Published: September 30, 2023
ATP6V0C Is Associated With Febrile Seizures and Epilepsy With Febrile Seizures Plus.
Journal: Frontiers in molecular neuroscience
Published: March 04, 2022
Novel PANK2 Mutations in Patients With Pantothenate Kinase-Associated Neurodegeneration and the Genotype-Phenotype Correlation.
Journal: Frontiers in aging neuroscience
Published: January 05, 2022
Clinical and Functional Features of Epilepsy-Associated In-Frame Deletion Variants in SCN1A.
Journal: Frontiers in molecular neuroscience
Published: December 04, 2021
HLA-B*13:01 as a Risk Allele for Antiepileptic Drugs-Induced Cutaneous Adverse Reactions: Higher Risk for Cross-Reactivity?
Journal: Frontiers in neurology
Published: July 17, 2018
A Point Mutation in SCN1A 5' Genomic Region Decreases the Promoter Activity and Is Associated with Mild Epilepsy and Seizure Aggravation Induced by Antiepileptic Drug.
Journal: Molecular neurobiology
Published: December 09, 2015
Showing 1-11 of 11
Last Updated: 09/26/2026