Xuelian He
12PUBLICATIONS
3CO-AUTHORS
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Publications (12)
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|Dec 23, 2025
Clinical and genetic characterization of congenital disorders of glycosylation in 20 Chinese patients.Peiwei Zhao, Li Tan, Qingjie Meng
|Oct 03, 2024
Analysis of epilepsy-associated variants in HCN3 - Functional implications and clinical observations.Peiwei Zhao, Hongbo Xiong, Gunagtao Kuang
|Jan 30, 2024
Activated phosphoinositide 3-kinase δ syndrome caused by PIK3CD mutations: expanding the phenotype.Peiwei Zhao, Juan Huang, Huicong Fu
|Feb 21, 2023
Clinical features of CNOT3-associated neurodevelopmental disorder in three Chinese patients.Peiwei Zhao, Qingjie Meng, Chunhui Wan
|Jan 05, 2023
Variants in BSN gene associated with epilepsy with favourable outcome.Tingting Ye, Jiwei Zhang, Jie Wang
|Oct 17, 2022
A novel variant in the HX repeat motif of ATN1 in a Chinese patient with CHEDDA syndrome and literature review.Sukun Luo, Yanqiu Hu, Ping Xiong
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