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KCNQ2 gene

Discuss publications and research concerning the KCNQ2 gene.

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Related literature

Comprehensive Pathologic and Genetic Investigation of Four Young Adults with a Short QT Interval and Sudden Unexpected Death.
KCNQ2
Self-limited Neonatal Epilepsy associated with global developmental delay and high-threshold sensory profile: A novel KCNQ3 de novo variant unusually located in the voltage sensor S4 segment of the Kv7.3 channel subunit.
KCNQ2
Biophysical and structural mechanisms of epilepsy-associated mutations in the S4-S5 Linker of KCNQ2 channels.
KCNQ2
Human iPSC-derived glutamatergic neurons with pathogenic KCNQ2 variants display hyperactive bursting phenotypes.
KCNQ2
Familial KCNQ2 mutation: a psychiatric perspective.
KCNQ2
One drug-sensitive subunit is sufficient for a near-maximal retigabine effect in KCNQ channels.
KCNQ2
Four drug-sensitive subunits are required for maximal effect of a voltage sensor-targeted KCNQ opener.
KCNQ2
Neonatal Alexander Disease: Novel GFAP Mutation and Comparison to Previously Published Cases.
KCNQ2
Genetic etiologies of the electrical status epilepticus during slow wave sleep: systematic review.
KCNQ2
Diagnostic work-up and rehabilitation of cerebral visual impairment in infancy: A case of epileptic perinatal encephalopathy due to KCNQ2-related channelopathy
KCNQ2

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