Autosomal Dominant Lateral Temporal Epilepsy: Clinical Spectrum, New Epitempin Mutations, and Genetic Heterogeneity in Seven European Families-Reference-Cited by-同舟云学术

Autosomal Dominant Lateral Temporal Epilepsy: Clinical Spectrum, New Epitempin Mutations, and Genetic Heterogeneity in Seven European Families

Published:2003-09-22 Issue:10 Volume:44 Page:1289-1297
ISSN:0013-9580
Container-title:Epilepsia
language:en
Short-container-title:

Author:

Michelucci Roberto,Poza Juan Jose,Sofia Vito,Feo Maria Rita de,Binelli Simona,Bisulli Francesca,Scudellaro Evan,Simionati Barbara,Zimbello Rosanna,D'Orsi Giuseppe,Passarelli Daniela,Avoni Patrizia,Avanzini Giuliano,Tinuper Paolo,Biondi Roberto,Valle Giorgio,Mautner Victor F.,Stephani Ulrich,Tassinari Carlo Alberto,Moschonas Nicholas K.,Siebert Reiner,Munain Adolpho Lopez de,Perez-Tur Jordi,Nobile Carlo

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1046/j.1528-1157.2003.20003.x/fullpdf

Reference26 articles.

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2. Autosomal dominant lateral temporal epilepsy: clinical and genetic study of a large Basque pedigree linked to chromosome 10q;Poza;Ann Neurol,1999

3. Familial temporal lobe epilepsy with aphasic seizures and linkage to chromosome 10q22-q24;Brodtkorb;Epilepsia,2002

4. Supporting evidence of a gene for partial epilepsy on 10q;Mautner;Neurogenetics,2000

5. Autosomal dominant partial epilepsy with auditory features: description of a new family;Michelucci;Epilepsia,2000

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