📣 Help Shape the Future of UKRI's Gateway to Research (GtR)

We're improving UKRI's Gateway to Research and are seeking your input! If you would be interested in being interviewed about the improvements we're making and to have your say about how we can make GtR more user-friendly, impactful, and effective for the Research and Innovation community, please email gateway@ukri.org.

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