Absence seizures arising from a mutation that causes selective loss of AMPA receptors within thalamocortical networks
KCNQ2 gene
Functional consequences of the R227Q and R230C/S/H variants in KCNQ3.... | Download Scientific Diagram
Kcnq3-Related Disorders disease: Malacards - Research Articles, Drugs, Genes, Clinical Trials
KCNQ3 siRNA (h), shRNA and Lentiviral Particle Gene Silencers | SCBT - Santa Cruz Biotechnology
KCNQ gene family members act as both tumor suppressors and oncogenes in gastrointestinal cancers | bioRxiv
KCNQ3 Gene - GeneCards | KCNQ3 Protein | KCNQ3 Antibody
Enigmatic encephalopathies | μNEURO | University of Antwerp
THE ROLE OF POTASSIUM CHANNELS IN THE PATHOGENESIS OF GASTROINTESTINAL CANCERS AND THERAPEUTIC POTENTIAL | bioRxiv
KCNQ3 siRNA (h): sc-42501
Transcriptional Control of KCNQ Channel Genes and the Regulation of Neuronal Excitability | Journal of Neuroscience
Gene: KCNQ3 (ENSG00000184156) - Summary - Homo_sapiens - Ensembl genome browser 109
Oral KCNQ2/3 Potassium Channel Opener for Epilepsy Treatment - Protheragen
Human KCNQ3 cDNA ORF Clone, untagged, HG18537-UT | Sino Biological
KCNQ2/KCNQ3 K+ channels and the molecular pathogenesis of epilepsy: implications for therapy: Trends in Neurosciences
KCNQ2 and KCNQ3 Potassium Channel Subunits: Molecular Correlates of the M-Channel | Science
KCNQ3 is the principal target of retigabine in CA1 and subicular excitatory neurons | Journal of Neurophysiology
KCNQ2- and KCNQ3-Associated Epilepsy
John Libbey Eurotext - Epileptic Disorders - Benign familial infantile epilepsy associated with KCNQ3 mutation: a rare occurrence or an underestimated event?
KCNQ3 (potassium voltage-gated channel subfamily Q member 3) | Gene Report | BioGPS
A novel mutation of KCNQ3 gene in a Chinese family with benign familial neonatal convulsions - ScienceDirect
KvLQT3 - Wikipedia
Brain Sciences | Free Full-Text | Neonatal Seizures: An Overview of Genetic Causes and Treatment Options
Gene: KCNQ3 (ENSG00000184156) - Summary - Homo_sapiens - GRCh37 Archive browser 109
Protein structure - KCNQ3 - The Human Protein Atlas
Location of 29 mutations in the KCNQ2 gene and three mutations in the... | Download Scientific Diagram
Frontiers | A Novel Kv7.3 Variant in the Voltage-Sensing S4 Segment in a Family With Benign Neonatal Epilepsy: Functional Characterization and in vitro Rescue by β-Hydroxybutyrate
