Exon‐disrupting deletions of <scp><i>NRXN1</i></scp> in idiopathic generalized epilepsy - Concepedia

Concepedia

Publication | Open Access

Exon‐disrupting deletions of <scp><i>NRXN1</i></scp> in idiopathic generalized epilepsy

DOI Full Paper Access

67

Citations

26

References

2013

Year

Rikke S. Møller, Yvonne Weber, Laura L. Klitten, Holger Trucks, Hiltrud Muhle, Wolfram S. Kunz, Heather C. Mefford, Andre Franke, Monika Kautza, Peter Wolf,

Abstract

We conclude that exon-disrupting deletions of NRXN1 represent a genetic risk factor in the genetically complex predisposition of common IGE syndromes.

References

	Year	Citations

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