Mutant GABA(A) receptor gamma2-subunit in childhood absence epilepsy and febrile seizures (Q28186159)

From Wikidata

Jump to navigation Jump to search

scientific article (publication date: May 2001)

edit

Language	Label	Description	Also known as
English	Mutant GABA(A) receptor gamma2-subunit in childhood absence epilepsy and febrile seizures	scientific article (publication date: May 2001)

Statements

instance of

scholarly article

0 references

title

Mutant GABA(A) receptor gamma2-subunit in childhood absence epilepsy and febrile seizures (English)

0 references

main subject

childhood absence epilepsy

1 reference

based on heuristic

inferred from title

author

Carla Marini

1 reference

stated in

ORCID Public Data File 2021

author name string

R H Wallace

series ordinal

1

0 references

C Marini

series ordinal

2

0 references

S Petrou

series ordinal

3

0 references

L A Harkin

series ordinal

4

0 references

D N Bowser

series ordinal

5

0 references

R G Panchal

series ordinal

6

0 references

D A Williams

series ordinal

7

0 references

G R Sutherland

series ordinal

8

0 references

J C Mulley

series ordinal

9

0 references

I E Scheffer

series ordinal

10

0 references

S F Berkovic

series ordinal

11

0 references

language of work or name

English

0 references

publication date

May 2001

0 references

published in

Nature Genetics

0 references

volume

28

0 references

issue

1

0 references

page(s)

49-52

0 references

cites work

Incidence of epilepsy and unprovoked seizures in Rochester, Minnesota: 1935-1984.

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG0501-49

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Proposal for revised classification of epilepsies and epileptic syndromes. Commission on Classification and Terminology of the International League Against Epilepsy

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG0501-49

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

A missense mutation in the neuronal nicotinic acetylcholine receptor alpha 4 subunit is associated with autosomal dominant nocturnal frontal lobe epilepsy

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG0501-49

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

A potassium channel mutation in neonatal human epilepsy

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG0501-49

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG0501-49

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%2FNG0501-49

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Febrile seizures and generalized epilepsy associated with a mutation in the Na+-channel beta1 subunit gene SCN1B.

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG0501-49

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Mutations of SCN1A, encoding a neuronal sodium channel, in two families with GEFS+2

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG0501-49

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

The nicotinic receptor beta 2 subunit is mutant in nocturnal frontal lobe epilepsy

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG0501-49

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Genetics of the epilepsies

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG0501-49

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Exclusion of linkage between idiopathic generalized epilepsies and the GABAA receptor alpha 1 and gamma 2 subunit gene cluster on chromosome 5.

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG0501-49

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Association analysis of exonic variants of the gene encoding the GABAB receptor and idiopathic generalized epilepsy

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG0501-49

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Childhood absence epilepsy with tonic-clonic seizures and electroencephalogram 3-4-Hz spike and multispike-slow wave complexes: linkage to chromosome 8q24.

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG0501-49

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Possible association between childhood absence epilepsy and the gene encoding GABRB3

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG0501-49

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Concordance of clinical forms of epilepsy in families with several affected members. Italian League Against Epilepsy Genetic Collaborative Group

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG0501-49

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Functional and molecular distinction between recombinant rat GABAA receptor subtypes by Zn2+

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG0501-49

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Febrile seizures: treatment and prognosis

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG0501-49

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

GABA and epileptogenesis

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG0501-49

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Thalamocortical oscillations in the sleeping and aroused brain

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG0501-49

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Developmental changes in human γ‐aminobutyric acida receptor subunit composition

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG0501-49

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Generalized epilepsy with febrile seizures plus. A genetic disorder with heterogeneous clinical phenotypes

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG0501-49

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Avoiding recomputation in linkage analysis.

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG0501-49

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

DOI

10.1038/NG0501-49

0 references

10.1038/88259

1 reference

stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

2527069

OpenCitations bibliographic resource ID

2527069

1 reference

stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

2527069

PubMed publication ID

11326275

1 reference

stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

2527069

 

Sitelinks

Wikipedia(0 entries)

edit

Wikibooks(0 entries)

edit

Wikinews(0 entries)

edit

Wikiquote(0 entries)

edit

Wikisource(0 entries)

edit

Wikiversity(0 entries)

edit

Wikivoyage(0 entries)

edit

Wiktionary(0 entries)

edit

Multilingual sites(0 entries)

edit

Retrieved from "https://www.wikidata.org/w/index.php?title=Q28186159&oldid=2177493311"