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English
A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy family
scientific journal article
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instance of
scholarly article
1 reference
stated in
PubMed
PubMed ID
9425900
retrieved
3 January 2017
title
A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy family
(English)
1 reference
stated in
PubMed
PubMed ID
9425900
retrieved
3 January 2017
main subject
idiopathy
0 references
chemical synaptic transmission
1 reference
stated in
GOA release 2020-03-11
potassium
1 reference
based on heuristic
inferred from title
author
Carole Charlier
object named as
C. Charlier
series ordinal
1
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author name string
N. A. Singh
series ordinal
2
1 reference
stated in
PubMed
PubMed ID
9425900
retrieved
3 January 2017
S. G. Ryan
series ordinal
3
1 reference
stated in
PubMed
PubMed ID
9425900
retrieved
3 January 2017
T. B. Lewis
series ordinal
4
1 reference
stated in
PubMed
PubMed ID
9425900
retrieved
3 January 2017
B. E. Reus
series ordinal
5
1 reference
stated in
PubMed
PubMed ID
9425900
retrieved
3 January 2017
R. J. Leach
series ordinal
6
1 reference
stated in
PubMed
PubMed ID
9425900
retrieved
3 January 2017
M. Leppert
series ordinal
7
1 reference
stated in
PubMed
PubMed ID
9425900
retrieved
3 January 2017
language of work or name
English
0 references
publication date
1 January 1998
1 reference
stated in
PubMed
PubMed ID
9425900
retrieved
3 January 2017
published in
Nature Genetics
1 reference
stated in
PubMed
PubMed ID
9425900
retrieved
3 January 2017
volume
18
1 reference
stated in
PubMed
PubMed ID
9425900
retrieved
3 January 2017
page(s)
53–55
1 reference
stated in
PubMed
PubMed ID
9425900
retrieved
3 January 2017
issue
1
1 reference
stated in
PubMed
PubMed ID
9425900
retrieved
3 January 2017
exact match
https://scigraph.springernature.com/pub.10.1038/ng0198-53
0 references
cites work
Basic local alignment search tool
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0198-53
retrieved
21 January 2018
Idiopathic generalized epilepsy of adolescence: are the syndromes clinically distinct?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0198-53
retrieved
21 January 2018
Seizure characteristics in chromosome 20 benign familial neonatal convulsions
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0198-53
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The epidemiology of epilepsy in Rochester, Minnesota, 1935 through 1967
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0198-53
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Benign familial neonatal convulsions: Evidence for clinical and genetic heterogeneity
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0198-53
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Benign familial neonatal convulsions linked to genetic markers on chromosome 20.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0198-53
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Confirmation of linkage of benign familial neonatal convulsions to D20S19 and D20S20.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0198-53
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Benign familial neonatal convulsions: confirmation of genetic heterogeneity and further evidence for a second locus on chromosome 8q
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0198-53
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newborns
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0198-53
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Eight potassium channel families revealed by the C. elegans genome project.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0198-53
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A radiation hybrid map of 40 loci for the distal long arm of human chromosome 8.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0198-53
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0198-53
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0198-53
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Construction and characterization of a normalized cDNA library
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0198-53
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
NIGMS human/rodent somatic cell hybrid mapping panels 1 and 2.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0198-53
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
KvLQT1, a voltage-gated potassium channel responsible for human cardiac arrhythmias
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0198-53
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A comprehensive genetic map of the human genome based on 5,264 microsatellites
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0198-53
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mapping of genes predisposing to idiopathic generalized epilepsy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0198-53
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Possible association of a silent polymorphism in the neuronal nicotinic acetylcholine receptor subunit alpha4 with common idiopathic generalized epilepsies
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0198-53
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Stargazer: a new neurological mutant on chromosome 15 in the mouse with prolonged cortical seizures.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0198-53
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genetic and physical maps of the stargazer locus on mouse chromosome 15
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0198-53
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Searching for human epilepsy genes: a progress report.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0198-53
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1038/NG0198-53
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
1335545
OpenCitations bibliographic resource ID
1335545
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
1335545
PubMed ID
9425900
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
1335545
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