Genome scan of idiopathic generalized epilepsy: Evidence for major susceptibility gene and modifying genes influencing the seizure type-Reference-Cited by-同舟云学术

Genome scan of idiopathic generalized epilepsy: Evidence for major susceptibility gene and modifying genes influencing the seizure type

Published:2001 Issue:3 Volume:49 Page:328-335
ISSN:0364-5134
Container-title:Annals of Neurology
language:en
Short-container-title:Ann Neurol.

Author:

Durner Martina,Keddache Mehdi A.,Tomasini Livia,Shinnar Shlomo,Resor Stanley R.,Cohen Jeffrey,Harden Cynthia,Moshe Solomon L.,Rosenbaum David,Kang Harriet,Ballaban-Gil Karen,Hertz Sharon,Labar Douglas R.,Luciano Daniel,Wallace Sibylle,Yohai David,Klotz Irene,Dicker Elisa,Greenberg David A.

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Reference40 articles.

1. Benign familial neonatal convulsions linked to genetic markers on chromosome 20

2. Febrile seizures and generalized epilepsy associated with a mutation in the Na+-channel ß1 subunit gene SCN1B

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

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

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

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