SOX11 variants cause a neurodevelopmental disorder with infrequent ocular malformations and hypogonadotropic hypogonadism and with distinct DNA methylation profile. (2022)
Attributed to:
UK Infrastructure for Large-scale Clinical Genomics Research
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1016/j.gim.2022.02.013
PubMed Identifier: 35341651
Publication URI: http://europepmc.org/abstract/MED/35341651
Type: Journal Article/Review
Volume: 24
Parent Publication: Genetics in medicine : official journal of the American College of Medical Genetics
Issue: 6
ISSN: 1098-3600