Heterozygous lamin B1 and lamin B2 variants cause primary microcephaly and define a novel laminopathy. (2021)
Attributed to:
The Wales Genomic Medicine Centre
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1038/s41436-020-00980-3
PubMed Identifier: 33033404
Publication URI: http://europepmc.org/abstract/MED/33033404
Type: Journal Article/Review
Volume: 23
Parent Publication: Genetics in medicine : official journal of the American College of Medical Genetics
Issue: 2
ISSN: 1098-3600