Heterozygous lamin B1 and lamin B2 variants cause primary microcephaly and define a novel laminopathy. (2021)

First Author: Parry DA
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