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No evidence for a role of CLCN2 variants in idiopathic generalized epilepsy

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No evidence for a role of CLCN2 variants in idiopathic generalized epilepsy (English)

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Thomas J Jentsch

6

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María I Niemeyer

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1

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L Pablo Cid

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2

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Francisco V Sepúlveda

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3

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Judith Blanz

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4

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Muriel Auberson

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5

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language of work or name

English

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publication date

January 2010

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published in

Nature Genetics

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volume

42

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issue

1

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page(s)

3-3

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exact match

https://scigraph.springernature.com/pub.10.1038/ng0110-3

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cites work

Mutations in CLCN2 encoding a voltage-gated chloride channel are associated with idiopathic generalized epilepsies

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https://api.crossref.org/works/10.1038%2FNG0110-3

retrieved

21 January 2018

Functional evaluation of human ClC-2 chloride channel mutations associated with idiopathic generalized epilepsies

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Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG0110-3

retrieved

21 January 2018

Leukoencephalopathy upon disruption of the chloride channel ClC-2.

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reference URL

https://api.crossref.org/works/10.1038%2FNG0110-3

retrieved

21 January 2018

Mutations and polymorphisms of the CLCN2 gene in idiopathic epilepsy

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Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG0110-3

retrieved

21 January 2018

Male germ cells and photoreceptors, both dependent on close cell-cell interactions, degenerate upon ClC-2 Cl(-) channel disruption

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reference URL

https://api.crossref.org/works/10.1038%2FNG0110-3

retrieved

21 January 2018

CLC Chloride Channels and Transporters: From Genes to Protein Structure, Pathology and Physiology

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reference URL

https://api.crossref.org/works/10.1038%2FNG0110-3

retrieved

21 January 2018

Chloride channelopathies

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stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG0110-3

retrieved

21 January 2018

CLCN2 variants in idiopathic generalized epilepsy

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/20037607

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12 December 2020

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(Q56974903)

No evidence for a role of CLCN2 variants in idiopathic generalized epilepsy

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