A novel de novo truncating variant in a Hungarian patient with CTNNB1 neurodevelopmental disorder.
- Resource Type
- Case Study
- Source
- BMC Pediatrics; 1/15/2024, Vol. 24 Issue 1, p1-6, 6p
- Subject
STRABISMUS CELL determination FETAL growth retardation NEURAL development CONSCIOUSNESS raising GENETIC testing - Language
- ISSN
- 14712431