Low penetrance of autosomal dominant lateral temporal epilepsy in Italian families without LGI1 mutations. (Q46333169)

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29 February 2020

title

Low penetrance of autosomal dominant lateral temporal epilepsy in Italian families without LGI1 mutations (English)

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Lilia Volpi

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Patrizia Riguzzi

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Carlo Di Bonaventura

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Vito Sofia

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Lia Santulli

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Pasquale Striano

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Gabriella Egeo

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Arturo de Falco

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Simona Binelli

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Clementina Boniver

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Marco Marchini

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Oriano Mecarelli

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Patrizia Pulitano

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Angela la Neve

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Paola Banfi

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Emanuela Dazzo

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Manuela Fanciulli

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Yerma Bartolini

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Anna Teresa Giallonardo

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Salvatore Striano

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Carlo Nobile

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Fabrizio A de Falco

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publication date

26 April 2013

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volume

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issue

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page(s)

1288-1297

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On the use of familial aggregation in population-based case probands for calculating penetrance

29 February 2020

cites work

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LGI1 mutations in temporal lobe epilepsies

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Idiopathic partial epilepsy with auditory features (IPEAF): a clinical and genetic study of 53 sporadic cases.

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Familial temporal lobe epilepsy with aphasic seizures and linkage to chromosome 10q22-q24.

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Speech-induced aphasic seizures in epilepsy caused by LGI1 mutation

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Two novel epilepsy-linked mutations leading to a loss of function of LGI1.

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Absence of mutations in the LGI1 receptor ADAM22 gene in autosomal dominant lateral temporal epilepsy

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Drug resistant ADLTE and recurrent partial status epilepticus with dysphasic features in a family with a novel LGI1mutation: electroclinical, genetic, and EEG/fMRI findings

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LGI1 microdeletion in autosomal dominant lateral temporal epilepsy.

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LGI1 is mutated in familial temporal lobe epilepsy characterized by aphasic seizures

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Autosomal dominant lateral temporal epilepsy: two families with novel mutations in the LGI1 gene

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Evaluation of depression risk in LGI1 mutation carriers

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

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Mutations in LGI1 gene in Japanese families with autosomal dominant lateral temporal lobe epilepsy: the first report from Asian families

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Autosomal dominant lateral temporal epilepsy: clinical spectrum, new epitempin mutations, and genetic heterogeneity in seven European families

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Mutations in the LGI1/Epitempin gene on 10q24 cause autosomal dominant lateral temporal epilepsy

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Localization of a gene for partial epilepsy to chromosome 10q

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LGI1 mutations in autosomal dominant partial epilepsy with auditory features

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Abnormal phonologic processing in familial lateral temporal lobe epilepsy due to a new LGI1 mutation

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