Comprehensive study of 28 individuals with SIN3A-related disorder underscoring the associated mild cognitive and distinctive facial phenotype. (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/10.1038/s41431-020-00769-7
PubMed Identifier: 33437032
Publication URI: http://europepmc.org/abstract/MED/33437032
Type: Journal Article/Review
Volume: 29
Parent Publication: European journal of human genetics : EJHG
Issue: 4
ISSN: 1018-4813