Partial epilepsy with pericentral spikes: A new familial epilepsy syndrome with evidence for linkage to chromosome 4p15-Reference-Cited by-同舟云学术

Partial epilepsy with pericentral spikes: A new familial epilepsy syndrome with evidence for linkage to chromosome 4p15

Published:2002-05-23 Issue:6 Volume:51 Page:740-749
ISSN:0364-5134
Container-title:Annals of Neurology
language:en
Short-container-title:Ann Neurol.

Author:

Kinton Lucy,Johnson Michael R.,Smith Shelagh J. M.,Farrell Fiona,Stevens John,Rance James B.,Claudino Angelica M.,Duncan John S.,Davis Mary B.,Wood Nicholas W.,Sander Josemir W. A.

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Reference48 articles.

1. A missense mutation in the neuronal nicotinic acetylcholine receptor α4 subunit is associated with autosomal dominant nocturnal frontal lobe epilepsy

2. The nicotinic receptor β2 subunit is mutant in nocturnal frontal lobe epilepsy

3. A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newborns

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

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

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