The clinical phenotype of autosomal dominant lateral temporal lobe epilepsy related to reelin mutations-Reference-Cited by-同舟云学术

The clinical phenotype of autosomal dominant lateral temporal lobe epilepsy related to reelin mutations

Published:2017-03 Issue: Volume:68 Page:103-107
ISSN:1525-5050
Container-title:Epilepsy & Behavior
language:en
Short-container-title:Epilepsy & Behavior

Author:

Michelucci Roberto,Pulitano Patrizia,Di Bonaventura Carlo,Binelli Simona,Luisi Concetta,Pasini Elena,Striano Salvatore,Striano Pasquale,Coppola Giangennaro,La Neve Angela,Giallonardo Anna Teresa,Mecarelli Oriano,Serioli Elena,Dazzo Emanuela,Fanciulli Manuela,Nobile Carlo

Funder

Genetics Commission of the Italian League Against Epilepsy

Telethon Foundation

Publisher

Elsevier BV

Subject

Behavioral Neuroscience,Clinical Neurology,Neurology

Reference18 articles.

1. Localization of a gene for partial epilepsy to chromosome 10q;Ottman;Nat Genet,1995

2. Autosomal dominant lateral temporal epilepsy: clinical spectrum, new epitempin mutations, and genetic heterogeneity in seven European families;Michelucci;Epilepsia,2003

3. Mutations in LGI1 cause autosomal-dominant partial epilepsy with auditory features;Kalachikov;Nat Genet,2002

4. Mutations in the LGI1/Epitempin gene on 10q24 cause autosomal dominant lateral temporal epilepsy;Morante-Redolat;Hum Mol Genet,2002

5. Low penetrance of autosomal dominant lateral temporal epilepsy in Italian families without LGI1 mutations;Michelucci;Epilepsia,2013

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