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Improving diagnosis and broadening the phenotypes in early-onset seizure and severe developmental delay disorders through gene panel analysis. (2016)

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1136/jmedgenet-2015-103263

PubMed Identifier: 26993267

Publication URI: http://europepmc.org/abstract/MED/26993267

Type: Journal Article/Review

Volume: 53

Parent Publication: Journal of medical genetics

Issue: 5

ISSN: 0022-2593