(Q57905599)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21777232%20AND%20SRC:MED&resulttype=core&format=json

8 February 2020

title

Investigation of the 15q13.3 CNV as a genetic modifier for familial epilepsies with variable phenotypes (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21777232%20AND%20SRC:MED&resulttype=core&format=json

8 February 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21777232%20AND%20SRC:MED&resulttype=core&format=json

8 February 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21777232%20AND%20SRC:MED&resulttype=core&format=json

8 February 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21777232%20AND%20SRC:MED&resulttype=core&format=json

8 February 2020

Tarishi Desai

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21777232%20AND%20SRC:MED&resulttype=core&format=json

8 February 2020

John C Mulley

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21777232%20AND%20SRC:MED&resulttype=core&format=json

8 February 2020

Marta A Bayly

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21777232%20AND%20SRC:MED&resulttype=core&format=json

8 February 2020

Bronwyn E Grinton

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21777232%20AND%20SRC:MED&resulttype=core&format=json

8 February 2020

Danya F Vears

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21777232%20AND%20SRC:MED&resulttype=core&format=json

8 February 2020

publication date

21 July 2011

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21777232%20AND%20SRC:MED&resulttype=core&format=json

8 February 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21777232%20AND%20SRC:MED&resulttype=core&format=json

8 February 2020

volume

1 reference

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8 February 2020

issue

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21777232%20AND%20SRC:MED&resulttype=core&format=json

8 February 2020

page(s)

e139-42

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21777232%20AND%20SRC:MED&resulttype=core&format=json

Genetic modifiers affecting severity of epilepsy caused by mutation of sodium channel Scn2a.

8 February 2020

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2011.03188.X

Fine mapping of an epilepsy modifier gene on mouse Chromosome 19.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2011.03188.X

Familial and sporadic 15q13.3 microdeletions in idiopathic generalized epilepsy: precedent for disorders with complex inheritance

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2011.03188.X

Neuronal voltage-gated ion channels are genetic modifiers of generalized epilepsy with febrile seizures plus

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2011.03188.X

15q13.3 microdeletions increase risk of idiopathic generalized epilepsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2011.03188.X

Genetically complex epilepsies, copy number variants and syndrome constellations

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2011.03188.X

Susceptibility genes for complex epilepsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2011.03188.X

A small recurrent deletion within 15q13.3 is associated with a range of neurodevelopmental phenotypes

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2011.03188.X

A role of SCN9A in human epilepsies, as a cause of febrile seizures and as a potential modifier of Dravet syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2011.03188.X

Reduced sodium current in GABAergic interneurons in a mouse model of severe myoclonic epilepsy in infancy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2011.03188.X

10.1111/J.1528-1167.2011.03188.X

21 January 2018

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21777232%20AND%20SRC:MED&resulttype=core&format=json

8 February 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21777232%20AND%20SRC:MED&resulttype=core&format=json