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