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PLS3 whole gene deletion as a cause of X-linked osteoporosis: Clinical report with review of published PLS3 literature. (2023)

First Author: Apperley LJ

Attributed to: Unravelling the role of NBAS in skeletal development: towards treatment for NBAS-related human phenotype funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1097/mcd.0000000000000442

PubMed Identifier: 36503925

Publication URI: http://europepmc.org/abstract/MED/36503925

Type: Journal Article/Review

Volume: 32

Parent Publication: Clinical dysmorphology

Issue: 1

ISSN: 0962-8827