SOX11variants cause a neurodevelopmental disorder with infrequent ocular malformations and hypogonadotropic hypogonadism and with distinct DNA methylation profile
- Resource Type
- Article
- Source
- Genetics in Medicine; June 2022, Vol. 24 Issue: 6 p1261-1273, 13p
- Subject
- Language
- ISSN
- 10983600; 15300366