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Heterozygous Variants in KMT2E Cause a Spectrum of Neurodevelopmental Disorders and Epilepsy. (2019)

First Author: O'Donnell-Luria AH

Attributed to: The Northern Ireland Genomic Medicine Centre funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1016/j.ajhg.2019.03.021

PubMed Identifier: 31079897

Publication URI: http://europepmc.org/abstract/MED/31079897

Type: Journal Article/Review

Volume: 104

Parent Publication: American journal of human genetics

Issue: 6

ISSN: 0002-9297