Further evidence for attenuated phenotype with variants in the BMPER gene causing DSD: Case report 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/10.1016/j.ejmg.2022.104470
PubMed Identifier: 35240322
Publication URI: http://europepmc.org/abstract/MED/35240322
Type: Journal Article/Review
Volume: 65
Parent Publication: European journal of medical genetics
Issue: 4
ISSN: 1769-7212