Low penetrance and effect on protein secretion of LGI1 mutations causing autosomal dominant lateral temporal epilepsy-Reference-Cited by-同舟云学术

Low penetrance and effect on protein secretion of LGI1 mutations causing autosomal dominant lateral temporal epilepsy

Published:2011-04-19 Issue:7 Volume:52 Page:1258-1264
ISSN:0013-9580
Container-title:Epilepsia
language:en
Short-container-title:

Author:

Di Bonaventura Carlo,Operto Francesca F.,Busolin Giorgia,Egeo Gabriella,D’Aniello Alfredo,Vitello Libero,Smaniotto Gessica,Furlan Sandra,Diani Erica,Michelucci Roberto,Giallonardo Anna Teresa,Coppola Giangennaro,Nobile Carlo

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1528-1167.2011.03071.x/fullpdf

Reference19 articles.

1. A de novo LGI1 mutation in sporadic partial epilepsy with auditory features;Bisulli;Ann Neurol,2004

2. Structural and functional diversity in the leucine-rich repeat family of proteins;Buchanan;Prog Biophys Mol Biol,1996

3. The LGI1/Epitempin gene encodes two protein isoforms differentially expressed in human brain;Furlan;J Neurochem,2006

4. Amino acid difference formula to help explain protein evolution;Grantham;Science,1974

5. Evaluation of depression risk in LGI1 mutation carriers;Heiman;Epilepsia,2010

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