Patients' priorities and expectations on an EU registry for rare bone and mineral conditions. (2021)
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/10.1186/s13023-021-02069-9
PubMed Identifier: 34732217
Publication URI: http://europepmc.org/abstract/MED/34732217
Type: Journal Article/Review
Volume: 16
Parent Publication: Orphanet journal of rare diseases
Issue: 1
ISSN: 1750-1172