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Exome-wide analysis of mutational burden in patients with typical and atypical Rolandic epilepsy. (2018)

First Author: Bobbili DR

Attributed to: Regulatory interactions and Complex Phenotypes funded by BBSRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1038/s41431-017-0034-x

PubMed Identifier: 29358611

Publication URI: http://europepmc.org/abstract/MED/29358611

Type: Journal Article/Review

Volume: 26

Parent Publication: European journal of human genetics : EJHG

Issue: 2

ISSN: 1018-4813