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Research Article - De Novo KCNB1 Mutations in Epileptic Encephalopathy
RESEARCH ARTICLE - DE NOVO KCNB1 MUTATIONS IN INFANTILE EPILEPSY INHIBIT REPETITIVE NEURONAL FIRING
RESEARCH ARTICLE - A NOVEL EPILEPTIC ENCEPHALOPATHY MUTATION IN KCNB1 DISRUPTS KV2.1 ION SELECTIVITY, EXPRESSION, AND LOCALIZATION
Gamechanger for Epilepsy - New Center Develops Unique Collaborations To Advance Epilepsy Research
Researchers Discover New Genetic Cause of Rare, Complex Form of Epilepsy
RESEARCH ARTICLE - Functional Up-Regulation of KCNA Gene Family Expression in Murine Mesenteric Resistance Artery Smooth Musle
RESEARCH ARTICLE - NEURODEVELOPMENTAL DISORDERS CAUSED BY DE NOVO VARIANTS IN KCNB1 GENOTYPES AND PHENOTYPES
RESEARCH ARTICLE - KCNB1 MUTATIONS ASSOCIATED WITH VARIABLE NEURODEVELOPMENTAL DISORDER PHENOTYPES
RESEARCH ARTICLE - CLINICIAN'S GUIDE TO GENES ASSOCIATED WITH RETT-LIKE PHENOTYPES - INVESTIGATION OF A DANISH COHORT AND REVIEW OF THE LITERATURE
RESEARCH ARTICLE - LINOLEIC ACID BOTH ENHANCES ACTIVATION AND BLOCKS KV1.5 AND KV2.1 CHANNELS BY TWO SEPARATE MECHANISMS
RESEARCH ARTICLE - OXIDATION OF KCNB1 POTASSIUM CHANNELS CAUSES NEUROTOXICITY AND COGNITIVE IMPAIRMENT IN A MOUSE MODEL OF TRAUMATIC BRAIN INJURY
RESEARCH ARTICLE - OXIDATION OF KCNB1 K+ CHANNELS IN CENTRAL NERVOUS SYSTEM AND BEYOND
HIGH THROUGHPUT FUNCTIONAL ANALYSIS OF KCNB1 VARIANTS ASSOCIATED WITH EPILEPTIC ENCEPHALOPATHY TYPE 26 (AMERICAN EPILEPSY ASSOCIATION 2015)
Obligatory Heterotetramerization of thrEE PREVIOUSLY UNCHARACTERIZED KV CHANNEL A-SUBUNITS IDENTIFIED IN THE HUMAN GENOME
RESEARCH ARTICLE - MULTIPLE SINGLE-NUCLEOTIDE POLYMORPHISMS (SNPs) IN THE JAPANESE POPULATION IN SIX CANDIDATE GENES FOR LONG QT SYNDROME
NIH - U.S. National Library of Medicine - KCNB1 Genetics Home Reference
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