Severe neurodevelopmental disease caused by a homozygous TLK2 variant. (2020)
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1038/s41431-019-0519-x
PubMed Identifier: 31558842
Publication URI: http://europepmc.org/abstract/MED/31558842
Type: Journal Article/Review
Volume: 28
Parent Publication: European journal of human genetics : EJHG
Issue: 3
ISSN: 1018-4813