Expanding the phenotype of SETD5-related disorder and presenting a novel association with bone fragility. (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/10.1111/cge.14014
PubMed Identifier: 34169511
Publication URI: http://europepmc.org/abstract/MED/34169511
Type: Journal Article/Review
Volume: 100
Parent Publication: Clinical genetics
Issue: 3
ISSN: 0009-9163