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...

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Detalles Bibliográficos
Autores principales: Zhang, Wenyan, Yao, Ziming, Guo, Ruolan, Li, Haichong, Zhao, Shuang, Li, Wei, Zhang, Xuejun, Hao, Chanjuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Medicine
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

Internet

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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