Bin Tang
Key Laboratory Of Neurogenetics And Channelopathies Of Guangdong Province And The Ministry Of Education Of China, Changgang Dong Road
Guangzhou, 510000, China
Guangzhou, 510000, China
Last Updated: 09/26/2026
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Found 20 publications
The interaction of UBR4, LRP1, and OPHN1 in refractory epilepsy: Drosophila model to investigate the oligogenic effect on epilepsy.
Journal: Neurobiology of disease
Published: April 07, 2025
Characteristic spatial and frequency distribution of mutations in SCN1A.
Journal: Acta epileptologica
Published: April 08, 2024
IFIH1 variants are associated with generalised epilepsy preceded by febrile seizures.
Journal: Journal of medical genetics
Published: February 27, 2024
Corrigendum: ATP6V0C is associated with febrile seizures and epilepsy with febrile seizures plus.
Journal: Frontiers in molecular neuroscience
Published: February 14, 2024
HCFC1 variants in the proteolysis domain are associated with X-linked idiopathic partial epilepsy: Exploring the underlying mechanism.
Journal: Clinical and translational medicine
Published: December 20, 2022
ATP6V0C Is Associated With Febrile Seizures and Epilepsy With Febrile Seizures Plus.
Journal: Frontiers in molecular neuroscience
Published: March 04, 2022
ADGRV1 Variants in Febrile Seizures/Epilepsy With Antecedent Febrile Seizures and Their Associations With Audio-Visual Abnormalities.
Journal: Frontiers in molecular neuroscience
Published: January 28, 2022
Clinical and Functional Features of Epilepsy-Associated In-Frame Deletion Variants in SCN1A.
Journal: Frontiers in molecular neuroscience
Published: December 04, 2021
Critical Role of E1623 Residue in S3-S4 Loop of Nav1.1 Channel and Correlation Between Nature of Substitution and Functional Alteration.
Journal: Frontiers in molecular neuroscience
Published: October 19, 2021
GRIN2A Variants Associated With Idiopathic Generalized Epilepsies.
Journal: Frontiers in molecular neuroscience
Published: June 05, 2021
Differences in SCN1A intronic variants result in diverse aberrant splicing patterns and are related to the phenotypes of epilepsy with febrile seizures.
Journal: Epilepsy research
Published: January 25, 2021
Heterozygous PGM3 Variants Are Associated With Idiopathic Focal Epilepsy With Incomplete Penetrance.
Heterozygous PGM3 Variants Are Associated With Idiopathic Focal Epilepsy With Incomplete Penetrance.
Journal: Frontiers in genetics
Published: May 05, 2020
Last Updated: 09/26/2026