Data_Sheet_1_Heterozygous Recurrent Mutations Inducing Dysfunction of ROR2 Gene in Patients With Short Stature.docx

Purpose<p>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.</p>Methods<p>We retros...

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Main Author:	Baoheng Gui (10645124) (author)
Other Authors:	Chenxi Yu (4753110) (author), Xiaoxin Li (128947) (author), Sen Zhao (2232103) (author), Hengqiang Zhao (3449612) (author), Zihui Yan (8104445) (author), Xi Cheng (296756) (author), Jiachen Lin (9381248) (author), Haiyang Zheng (390545) (author), Jiashen Shao (10645127) (author), Zhengye Zhao (10645130) (author), Lina Zhao (178433) (author), Yuchen Niu (8104454) (author), Zhi Zhao (527379) (author), Huizi Wang (8700903) (author), Bobo Xie (3433766) (author), Xianda Wei (3492470) (author), Chunrong Gui (10645133) (author), Chuan Li (158692) (author), Shaoke Chen (612838) (author), Yi Wang (32470) (author), Yanning Song (2690959) (author), Chunxiu Gong (612836) (author), Terry Jianguo Zhang (8700906) (author)
Published:	2021
Subjects:	Cell Biology Marine Biology Cell Development, Proliferation and Death Cell Metabolism Cell Neurochemistry Cellular Interactions (incl. Adhesion, Matrix, Cell Wall) short stature ROR2 gene recurrent mutations dysfunction skeletal development
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Data_Sheet_1_Heterozygous Recurrent Mutations Inducing Dysfunction of ROR2 Gene in Patients With Short Stature.docx

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