(Q37861271)

24 August 2017

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title

Molecular and cellular basis: insights from experimental models of Dravet syndrome (English)

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24 August 2017

Kazuhiro Yamakawa

1

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24 August 2017

publication date

1 April 2011

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24 August 2017

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24 August 2017

volume

52 Suppl 2

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24 August 2017

page(s)

70-71

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De novo mutations in the sodium-channel gene SCN1A cause severe myoclonic epilepsy of infancy

24 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2011.03006.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2011.03006.X

Mutations of sodium channel alpha subunit type 1 (SCN1A) in intractable childhood epilepsies with frequent generalized tonic-clonic seizures

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2011.03006.X

Molecular basis of an inherited epilepsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2011.03006.X

Deletions of SCN1A 5' genomic region with promoter activity in Dravet syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2011.03006.X

Nav1.1 localizes to axons of parvalbumin-positive inhibitory interneurons: a circuit basis for epileptic seizures in mice carrying an Scn1a gene mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2011.03006.X

Noninactivating voltage-gated sodium channels in severe myoclonic epilepsy of infancy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2011.03006.X

Nav1.1 mutations cause febrile seizures associated with afebrile partial seizures

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2011.03006.X

Frequent mutations of SCN1A in severe myoclonic epilepsy in infancy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2011.03006.X

Nav1.1 channels with mutations of severe myoclonic epilepsy in infancy display attenuated currents.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2011.03006.X

Epilepsy and sodium channel gene mutations: gain or loss of function?

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2011.03006.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.1528-1167.2011.03006.X

10.1111/J.1528-1167.2011.03006.X

21 January 2018

Identifiers

DOI

1 reference

24 August 2017

1 reference