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SCN2A-Related Epilepsy: The Phenotypic Spectrum, Treatment and Prognosis

SCN2A-Related Epilepsy: The Phenotypic Spectrum, Treatment and Prognosis

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_306760eb36474d2c973dce80ed5b6858

SCN2A-Related Epilepsy: The Phenotypic Spectrum, Treatment and Prognosis

About this item

Full title

SCN2A-Related Epilepsy: The Phenotypic Spectrum, Treatment and Prognosis

Publisher

Switzerland: Frontiers Research Foundation

Journal title

Frontiers in molecular neuroscience, 2022-03, Vol.15, p.809951-809951

Language

English

Formats

Publication information

Publisher

Switzerland: Frontiers Research Foundation

More information

Scope and Contents

Contents

The aim of this study was to analyze the phenotypic spectrum, treatment, and prognosis of 72 Chinese children with
variants.
The
variants were detected by next-generation sequencing. All patients were followed up at a pediatric neurology clinic in our hospital or by telephone.
In 72 patients with
variants, the seizure onset age range...

Alternative Titles

Full title

SCN2A-Related Epilepsy: The Phenotypic Spectrum, Treatment and Prognosis

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_doaj_primary_oai_doaj_org_article_306760eb36474d2c973dce80ed5b6858

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_306760eb36474d2c973dce80ed5b6858

Other Identifiers

ISSN

1662-5099

E-ISSN

1662-5099

DOI

10.3389/fnmol.2022.809951

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