Literature DB >> 12771268

Novel LGI1 mutation in a family with autosomal dominant partial epilepsy with auditory features.

Evan Fertig1, Anne Lincoln, Andrea Martinuzzi, Richard H Mattson, Fuki M Hisama.   

Abstract

Autosomal dominant partial epilepsy with auditory features (ADPEAF) is a rare idiopathic epilepsy syndrome caused by mutations in the leucine-rich, glioma-inactivated 1 (LGI1) gene. The authors report that molecular genetic studies in seven affected family members identified a novel F318C substitution that alters a highly conserved residue in a predicted repeat domain of unknown function. This report suggests that this domain may participate in the development of the ADPEAF phenotype.

Entities:  

Mesh:

Substances:

Year:  2003        PMID: 12771268     DOI: 10.1212/01.wnl.0000063324.39980.4a

Source DB:  PubMed          Journal:  Neurology        ISSN: 0028-3878            Impact factor:   9.910


  11 in total

Review 1.  Autosomal dominant nocturnal frontal lobe epilepsy--a critical overview.

Authors:  Romina Combi; Leda Dalprà; Maria Luisa Tenchini; Luigi Ferini-Strambi
Journal:  J Neurol       Date:  2004-08       Impact factor: 4.849

Review 2.  Deja vu in neurology.

Authors:  Edward Wild
Journal:  J Neurol       Date:  2005-01       Impact factor: 4.849

3.  LGI1 gene mutation screening in sporadic partial epilepsy with auditory features.

Authors:  E Flex; A Pizzuti; C Di Bonaventura; S Douzgou; G Egeo; J Fattouch; M Manfredi; B Dallapiccola; A T Giallonardo
Journal:  J Neurol       Date:  2005-01       Impact factor: 4.849

Review 4.  LGI1: a gene involved in epileptogenesis and glioma progression?

Authors:  W Gu; E Brodtkorb; T Piepoli; G Finocchiaro; O K Steinlein
Journal:  Neurogenetics       Date:  2005-04-13       Impact factor: 2.660

5.  Domain-dependent clustering and genotype-phenotype analysis of LGI1 mutations in ADPEAF.

Authors:  Yuan-Yuan Ho; Iuliana Ionita-Laza; Ruth Ottman
Journal:  Neurology       Date:  2012-02-08       Impact factor: 9.910

6.  LGI1 mutations in autosomal dominant partial epilepsy with auditory features.

Authors:  R Ottman; M R Winawer; S Kalachikov; C Barker-Cummings; T C Gilliam; T A Pedley; W A Hauser
Journal:  Neurology       Date:  2004-04-13       Impact factor: 9.910

7.  Expression studies in gliomas and glial cells do not support a tumor suppressor role for LGI1.

Authors:  Tiziana Piepoli; Cemile Jakupoglu; Wenli Gu; Elena Lualdi; Blanca Suarez-Merino; Pietro L Poliani; Maria Grazia Cattaneo; Barbara Ortino; Dorota Goplen; Jian Wang; Rosa Mola; Francesca Inverardi; Carolina Frassoni; Rolf Bjerkvig; Ortrud Steinlein; Lucia M Vicentini; Oliver Brüstle; Gaetano Finocchiaro
Journal:  Neuro Oncol       Date:  2006-03-02       Impact factor: 12.300

8.  Penetrance of LGI1 mutations in autosomal dominant partial epilepsy with auditory features.

Authors:  Michael J Rosanoff; Ruth Ottman
Journal:  Neurology       Date:  2008-08-19       Impact factor: 9.910

9.  LGI1-associated epilepsy through altered ADAM23-dependent neuronal morphology.

Authors:  Katherine Owuor; Noam Y Harel; Dario J Englot; Fuki Hisama; Hal Blumenfeld; Stephen M Strittmatter
Journal:  Mol Cell Neurosci       Date:  2009-09-29       Impact factor: 4.314

10.  Genetics of temporal lobe epilepsy: a review.

Authors:  Annick Salzmann; Alain Malafosse
Journal:  Epilepsy Res Treat       Date:  2012-02-19
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.