(Q38046971)

27 August 2017

title

Duplication of the sodium channel gene cluster on 2q24 in children with early onset epilepsy (English)

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27 August 2017

author name string

Barbara Goeggel Simonetti

1

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27 August 2017

Claudine Rieubland

2

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27 August 2017

Carolina Courage

3

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27 August 2017

Susi Strozzi

4

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27 August 2017

Sibylle Tschumi

5

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27 August 2017

Sabina Gallati

6

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27 August 2017

Johannes R Lemke

7

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27 August 2017

publication date

27 September 2012

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27 August 2017

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27 August 2017

volume

53

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27 August 2017

issue

12

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27 August 2017

page(s)

2128-2134

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Newly diagnosed single unprovoked seizures and epilepsy in Stockholm, Sweden: First report from the Stockholm Incidence Registry of Epilepsy (SIRE).

27 August 2017

cites work

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https://api.crossref.org/works/10.1111%2FJ.1528-1167.2012.03676.X

Genetics of epilepsy syndromes starting in the first year of life

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2012.03676.X

Epilepsy and electroencephalographic anomalies in chromosome 2 aberrations. A review.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2012.03676.X

Mutation of sodium channel SCN3A in a patient with cryptogenic pediatric partial epilepsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2012.03676.X

Mice with targeted Slc4a10 gene disruption have small brain ventricles and show reduced neuronal excitability

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2012.03676.X

SCN1A duplications and deletions detected in Dravet syndrome: implications for molecular diagnosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2012.03676.X

The genetics of Dravet syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2012.03676.X

Infantile epilepsy associated with mosaic 2q24 duplication including SCN2A and SCN3A.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2012.03676.X

Epilepsies and epileptic syndromes starting in the neonatal period

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2012.03676.X

Familial neonatal seizures with intellectual disability caused by a microduplication of chromosome 2q24.3

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2012.03676.X

SCN2A Mutations and Benign Familial Neonatal-Infantile Seizures: The Phenotypic Spectrum

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2012.03676.X

10.1111/J.1528-1167.2012.03676.X

21 January 2018

Identifiers

DOI

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27 August 2017

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