Genotype-phenotypic association of heterozygous deletion of the TBX-6 gene in patients with congenital scoliosis
Introduction Congenital scoliosis is a multifactorial disease caused by abnormalities in vertebral development during embryogenesis. The TBX6 gene, located at locus 16p11.2, plays a key role in somitogenesis, and the heterozygous deletion is associated with the development of specific phenotypes o...
Saved in:
| Main Authors: | , , , , , , , |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
Russian Ilizarov Scientific Center for Restorative Traumatology and Orthopaedics
2025-06-01
|
| Series: | Гений oртопедии |
| Subjects: | |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|