Mutational burden and potential oligogenic model of TBX6‐mediated genes in congenital scoliosis

BACKGROUND: Congenital scoliosis (CS) is a spinal deformity due to vertebral malformations. Although insufficiency of TBX6 dosage contributes to a substantial proportion of CS, the molecular etiology for the majority of CS remains largely unknown. TBX6‐mediated genes involved in the process of somit...

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Dades bibliogràfiques
Publicat a:Mol Genet Genomic Med
Autors principals: Yang, Yang, Zhao, Sen, Zhang, Yuanqiang, Wang, Shengru, Shao, Jiashen, Liu, Bowen, Li, Yaqi, Yan, Zihui, Niu, Yuchen, Li, Xiaoxin, Wang, Lianlei, Ye, Yongyu, Weng, Xisheng, Wu, Zhihong, Zhang, Jianguo, Wu, Nan
Format: Artigo
Idioma:Inglês
Publicat: John Wiley and Sons Inc. 2020
Matèries:
Original Articles
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC7549550/
https://ncbi.nlm.nih.gov/pubmed/32815649
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mgg3.1453
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