📣 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.

Insertion Mutation in Tnfrsf11a Causes a Paget's Disease-Like Phenotype in Heterozygous Mice and Osteopetrosis in Homozygous Mice. (2021)

First Author: Alonso N

Attributed to: Centre for Integrated research into Musculoskeletal Ageing (CIMA) Renewal funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1002/jbmr.4288

PubMed Identifier: 33724536

Publication URI: http://europepmc.org/abstract/MED/33724536

Type: Journal Article/Review

Volume: 36

Parent Publication: Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research

Issue: 7

ISSN: 0884-0431