Heterozygous Recurrent Mutations Inducing Dysfunction of ROR2 Gene in Patients With Short Stature

PURPOSE: ROR2, a member of the ROR family, is essential for skeletal development as a receptor of Wnt5a. The present study aims to investigate the mutational spectrum of ROR2 in children with short stature and to identify the underlying molecular mechanisms. METHODS: We retrospectively analyzed clin...

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Detalles Bibliográficos
Autores principales: Gui, Baoheng, Yu, Chenxi, Li, Xiaoxin, Zhao, Sen, Zhao, Hengqiang, Yan, Zihui, Cheng, Xi, Lin, Jiachen, Zheng, Haiyang, Shao, Jiashen, Zhao, Zhengye, Zhao, Lina, Niu, Yuchen, Zhao, Zhi, Wang, Huizi, Xie, Bobo, Wei, Xianda, Gui, Chunrong, Li, Chuan, Chen, Shaoke, Wang, Yi, Song, Yanning, Gong, Chunxiu, Zhang, Terry Jianguo, Fan, Xin, Wu, Zhihong, Chen, Yujun, Wu, Nan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Cell and Developmental Biology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8080376/
https://www.ncbi.nlm.nih.gov/pubmed/33937263
http://dx.doi.org/10.3389/fcell.2021.661747

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8080376/
https://www.ncbi.nlm.nih.gov/pubmed/33937263
http://dx.doi.org/10.3389/fcell.2021.661747

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