Ultra-rare genetic variation in common epilepsies: a case-control sequencing study. (2017)

First Author: Epi4K Consortium

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1016/S1474-4422(16)30359-3

PubMed Identifier: 28102150

Publication URI: http://europepmc.org/abstract/MED/28102150

Type: Journal Article/Review

Volume: 16

Parent Publication: The Lancet. Neurology

Issue: 2

ISSN: 1474-4422