(Q28249219)

5

object named as

Jonathan L Haines

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author name string

Peter Hedera

1

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Bassel Abou-Khalil

2

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Amy E Crunk

3

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Kelly A Taylor

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

4

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language of work or name

English

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publication date

March 2004

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published in

Epilepsia

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volume

45

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page(s)

218-22

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issue

3

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cites work

1 reference

https://api.crossref.org/works/10.1111/J.0013-9580.2004.47203.X

A novel gene, LGI1, from 10q24 is rearranged and downregulated in malignant brain tumors

21 April 2017

1 reference

https://api.crossref.org/works/10.1111/J.0013-9580.2004.47203.X

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

21 April 2017

1 reference

https://api.crossref.org/works/10.1111/J.0013-9580.2004.47203.X

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

21 April 2017

1 reference

https://api.crossref.org/works/10.1111/J.0013-9580.2004.47203.X

The LGI1 gene involved in lateral temporal lobe epilepsy belongs to a new subfamily of leucine-rich repeat proteins

21 April 2017

1 reference

https://api.crossref.org/works/10.1111/J.0013-9580.2004.47203.X

A novel gene causing a mendelian audiogenic mouse epilepsy

21 April 2017

1 reference

https://api.crossref.org/works/10.1111/J.0013-9580.2004.47203.X

A nonsense mutation of the MASS1 gene in a family with febrile and afebrile seizures

21 April 2017

1 reference

https://api.crossref.org/works/10.1111/J.0013-9580.2004.47203.X

A common protein interaction domain links two recently identified epilepsy genes

21 April 2017

1 reference

https://api.crossref.org/works/10.1111/J.0013-9580.2004.47203.X

Autosomal dominant partial epilepsy with auditory features: defining the phenotype

21 April 2017

1 reference

https://api.crossref.org/works/10.1111%2FJ.0013-9580.2004.47203.X

Autosomal dominant lateral temporal epilepsy: clinical and genetic study of a large Basque pedigree linked to chromosome 10q.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.0013-9580.2004.47203.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.0013-9580.2004.47203.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.0013-9580.2004.47203.X

Proteins with leucine-rich repeats

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.0013-9580.2004.47203.X

Four new families with autosomal dominant partial epilepsy with auditory features: clinical description and linkage to chromosome 10q24.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.0013-9580.2004.47203.X