Familial Partial Epilepsy with Variable Foci: Clinical Features and Linkage to Chromosome 22q12-Reference-Cited by-同舟云学术

Familial Partial Epilepsy with Variable Foci: Clinical Features and Linkage to Chromosome 22q12

Published:2004-09 Issue:9 Volume:45 Page:1054-1060
ISSN:0013-9580
Container-title:Epilepsia
language:en
Short-container-title:Epilepsia

Author:

Berkovic Samuel F.,Serratosa Jose M.,Phillips Hilary A.,Xiong Lan,Andermann Eva,Diaz-Otero Fernando,Gomez-Garre Pilar,Martin Mercedes,Fernandez-Bullido Yolanda,Andermann Frederick,Lopes-Cendes Iscia,Dubeau Francois,Desbiens Richard,Scheffer Ingrid E.,Wallace Robyn H.,Mulley John C.,Pandolfo Massimo

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.0013-9580.2004.30502.x/fullpdf

Reference16 articles.

1. Genetics of the Epilepsies

2. Genetics of temporal lobe epilepsy

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

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

5. Mutations in LGI1 cause autosomal-dominant partial epilepsy with auditory features

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