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Five known tagging DLL3 SNPs are not associated with congenital scoliosis: A case–control association study in a Chinese Han population

Genetic etiology hypothesis is widely accepted in the development of congenital scoliosis (CS). The delta-like 3 (DLL3) gene, a member of the Notch signaling pathway, was implicated to contribute to human CS. In this study, a case–control association study was conducted to determine the association...

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Detalles Bibliográficos
Autores principales: Yang, Yong, Wang, Bing-Qiang, Wu, Zhi-Hong, Zhang, Hai-Yan, Qiu, Gui-Xing, Shen, Jian-Xiong, Zhang, Jian-Guo, Zhao, Yu, Wang, Yi-Peng, Fei, Qi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5265857/
https://www.ncbi.nlm.nih.gov/pubmed/27472720
http://dx.doi.org/10.1097/MD.0000000000004347

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