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Skeletal progenitor LRP1 deficiency causes severe and persistent skeletal defects with Wnt pathway dysregulation. (2025)

First Author: Alhashmi M

Attributed to: A comprehensive spatial analysis of active gene regulatory elements in the neural border during early development funded by BBSRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1038/s41413-024-00393-x

PubMed Identifier: 39865089

Publication URI: http://europepmc.org/abstract/MED/39865089

Type: Journal Article/Review

Volume: 13

Parent Publication: Bone research

Issue: 1

ISSN: 2095-4700