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Molecular identification of T-box transcription factor 6 and prognostic assessment in patients with congenital scoliosis: A single-center study
BACKGROUND: Congenital scoliosis (CS) is characterized by vertebral malformations. The precise etiology of CS is not fully defined. A compound inheritance of TBX6 was identified in 10% of patients with CS in Han Chinese and formed a distinguishable subtype named TBX6-associated congenital scoliosis...
Autores principales: | Zhang, Wenyan, Yao, Ziming, Guo, Ruolan, Li, Haichong, Zhao, Shuang, Li, Wei, Zhang, Xuejun, Hao, Chanjuan |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9403053/ https://www.ncbi.nlm.nih.gov/pubmed/36035411 http://dx.doi.org/10.3389/fmed.2022.941468 |
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