Expanding the phenotype of SPARC-related osteogenesis imperfecta: clinical findings in two patients with pathogenic variants in SPARC and literature review. (2022)
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/10.1136/jmedgenet-2021-107942
PubMed Identifier: 34462290
Publication URI: http://europepmc.org/abstract/MED/34462290
Type: Journal Article/Review
Volume: 59
Parent Publication: Journal of medical genetics
Issue: 8
ISSN: 0022-2593