Discover Community Create You

t/gene-kcnq3

KCNQ3 gene

Discuss publications and research concerning the KCNQ3 gene.

0 followers0 posts17 articles

All posts discussion question review note

Create the first post

Ask a question, share an idea or link scientific evidence.

Topic rules

Follow Noodle’s community and scientific integrity rules.

Moderators

Managed by the Noodle moderation team.

Related literature

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.
KCNQ3
Constitutive opening of the Kv7.2 pore activation gate causes KCNQ2-developmental encephalopathy.
KCNQ3
One drug-sensitive subunit is sufficient for a near-maximal retigabine effect in KCNQ channels.
KCNQ3
Four drug-sensitive subunits are required for maximal effect of a voltage sensor-targeted KCNQ opener.
KCNQ3
Novel genetic causes for cerebral visual impairment.
KCNQ3
Interaction between Common Genetic Variants and Total Fat Intake on Low-Density Lipoprotein Peak Particle Diameter: A Genome-Wide Association Study.
KCNQ3
A novel KCNQ3 gene mutation in a child with infantile convulsions and partial epilepsy with centrotemporal spikes.
KCNQ3
Potassium channel genes and benign familial neonatal epilepsy.
KCNQ3
Benign familial neonatal convulsions caused by mutation in KCNQ3, exon 6: a European case.
KCNQ3
KCNQ2 encephalopathy: emerging phenotype of a neonatal epileptic encephalopathy.
KCNQ3

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details