(Q28115034)

3 January 2017

title

A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy family (English)

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chemical synaptic transmission

3 January 2017

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GOA release 2020-03-11

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C. Charlier

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N. A. Singh

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3 January 2017

S. G. Ryan

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3 January 2017

T. B. Lewis

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3 January 2017

B. E. Reus

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3 January 2017

R. J. Leach

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3 January 2017

M. Leppert

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3 January 2017

language of work or name

English

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publication date

1 January 1998

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3 January 2017

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3 January 2017

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3 January 2017

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3 January 2017

page(s)

53–55

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Basic local alignment search tool

3 January 2017

cites work

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Idiopathic generalized epilepsy of adolescence: are the syndromes clinically distinct?

21 January 2018

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Seizure characteristics in chromosome 20 benign familial neonatal convulsions

21 January 2018

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7 January 2021

The epidemiology of epilepsy in Rochester, Minnesota, 1935 through 1967

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7 January 2021

Benign familial neonatal convulsions: Evidence for clinical and genetic heterogeneity

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7 January 2021

Benign familial neonatal convulsions linked to genetic markers on chromosome 20.

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7 January 2021

Confirmation of linkage of benign familial neonatal convulsions to D20S19 and D20S20.

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7 January 2021

Benign familial neonatal convulsions: confirmation of genetic heterogeneity and further evidence for a second locus on chromosome 8q

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7 January 2021

A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newborns

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7 January 2021

Eight potassium channel families revealed by the C. elegans genome project

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7 January 2021

A radiation hybrid map of 40 loci for the distal long arm of human chromosome 8.

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7 January 2021

Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias

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7 January 2021

A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome

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7 January 2021

Construction and characterization of a normalized cDNA library

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7 January 2021

NIGMS human/rodent somatic cell hybrid mapping panels 1 and 2.

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7 January 2021

KvLQT1, a voltage-gated potassium channel responsible for human cardiac arrhythmias

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7 January 2021

A comprehensive genetic map of the human genome based on 5,264 microsatellites

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7 January 2021

Mapping of genes predisposing to idiopathic generalized epilepsy

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7 January 2021

Possible association of a silent polymorphism in the neuronal nicotinic acetylcholine receptor subunit alpha4 with common idiopathic generalized epilepsies

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7 January 2021

Stargazer: a new neurological mutant on chromosome 15 in the mouse with prolonged cortical seizures.

1 reference

7 January 2021

Genetic and physical maps of the stargazer locus on mouse chromosome 15

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7 January 2021

Searching for human epilepsy genes: a progress report.

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7 January 2021

Identifiers

DOI

10.1038/NG0198-53

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Consolidated OpenCitations Corpus – April 2017

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Consolidated OpenCitations Corpus – April 2017

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Consolidated OpenCitations Corpus – April 2017