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Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic spikes

Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic spikes

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_1554948438

Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic spikes

About this item

Full title

Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic spikes

Publisher

New York: Nature Publishing Group US

Journal title

Nature genetics, 2013-09, Vol.45 (9), p.1067-1072

Language

English

Formats

Publication information

Publisher

New York: Nature Publishing Group US

More information

Scope and Contents

Contents

Sarah von Spiczak, Holger Lerche and colleagues identify mutations in
GRIN2A
that cause idiopathic focal epilepsy with rolandic spikes.
Idiopathic focal epilepsy (IFE) with rolandic spikes is the most common childhood epilepsy, comprising a phenotypic spectrum from rolandic epilepsy (also benign epilepsy with centrotemporal spikes, BECTS)...

Alternative Titles

Full title

Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic spikes

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_proquest_miscellaneous_1554948438

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_1554948438

Other Identifiers

ISSN

1061-4036

E-ISSN

1546-1718

DOI

10.1038/ng.2728

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