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De novo variants in neurodevelopmental disorders with epilepsy (2018)

First Author: Heyne H

Attributed to: Investigating the phenotype and genetic architecture of myoclonic astatic epilepsy funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1038/s41588-018-0143-7

PubMed Identifier: 29942082

Publication URI: http://europepmc.org/abstract/MED/29942082

Type: Journal Article/Review

Parent Publication: Nature Genetics

Issue: 7

ISSN: 1061-4036