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Novel GPC3 Gene Mutation in Simpson-Golabi-Behmel Syndrome with Endocrine Anomalies: A Case Report

By:
W Bu,  M Zhu,  S Li,  H Liu and  X Liu  
Open Access
|Jun 2022

Authors

W Bu

Department of Neurology, Shandong Provincial Qianfoshan Hospital, Weifang Medical University, Jinan, People's Republic of China

M Zhu

Department of Neurology, the First Affiliated Hospital of Shandong First Medical University & Shandong Provincial Qianfoshan Hospital, Jinan, People's Republic of China

S Li

Department of Neurology, the First Affiliated Hospital of Shandong First Medical University & Shandong Provincial Qianfoshan Hospital, Jinan, People's Republic of China

H Liu

Department of Neurology, Dingtao People's Hospital, Heze, People's Republic of China

X Liu

bosucn@163.com

Department of Neurology, the First Affiliated Hospital of Shandong First Medical University & Shandong Provincial Qianfoshan Hospital, Jinan, People's Republic of China
Language: English
Page range: 95 - 98
Published on: Jun 5, 2022
Published by: Macedonian Academy of Sciences and Arts
In partnership with: Paradigm Publishing Services
Publication frequency: 2 issues per year

© 2022 W Bu, M Zhu, S Li, H Liu, X Liu, published by Macedonian Academy of Sciences and Arts
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 License.