An interstitial duplication at 2q24.3 involving the SCN1A, SCN2A, SCN3A genes associated with infantile epilepsy.

American journal of medical genetics. Part A ·Vol. 155A ·No. 4 ·2011-04-00 ·Pages 920-3

Raymond G, Wohler E, Dinsmore C, Cox J, Johnston M, Batista D, Wang T

Abstract

暂无摘要

MeSH Terms

Adult Chromosome Banding Chromosome Duplication/genetics Chromosomes, Human, Pair 2/genetics Epilepsy/genetics Female Gene Order Humans In Situ Hybridization, Fluorescence Infant Male Mosaicism Oligonucleotide Array Sequence Analysis Sodium Channels/genetics

Chemicals

Sodium Channels

Authors & Affiliations

7 authors, click to expand affiliations / ORCID

Raymond Gerald

Kennedy Krieger Institute, Baltimore, Maryland, USA.

Wohler Elizabeth

Dinsmore Carolyn

Cox Jeanne

Johnston Michael

Batista Denise

Wang Tao

Article Info

Journal

American journal of medical genetics. Part A

Abbr.

Am J Med Genet A

ISSN

1552-4833

DOI

10.1002/ajmg.a.33929

Published

2011-04-00

Epub

2011-00-17

Pages

920-3

Language

English

Region

United States

NLM ID

101235741

Subset

External Links

PubMed source DOI: 10.1002/ajmg.a.33929 View journal details

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An interstitial duplication at 2q24.3 involving the SCN1A, SCN2A, SCN3A genes associated with infantile epilepsy.

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