Search Results - Jiancheng Jiao

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  1. 1
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    Novel GLDC Compound Heterozygous Variant Leading to Nonketotic Hyperglycinemia: Case Report and Literature Review by Yanyan Cao, Lingzhi Meng, Yudong Zhang, Jiancheng Jiao, Weicong Pu, Li Ma

    Published 2021
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  2. 2
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    Case report: A Chinese patient with glutathione synthetase deficiency and a novel glutathione synthase mutation by Xiaojiao Wu, Xiaojiao Wu, Jiancheng Jiao, Jiancheng Jiao, Yaofang Xia, Yaofang Xia, Xiaotong Yan, Xiaotong Yan, Zehao Liu, Zehao Liu, Yanyan Cao, Yanyan Cao, Li Ma, Li Ma

    Published 2023
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    High-Throughput Sequencing Reveals the Loss-of-Function Mutations in GALT Cause Recessive Classical Galactosemia by Lulu Li, Li Ma, Min Sun, Jiancheng Jiao, Yudong Zhang, Yue Tang, Nan Yang, Yuanyuan Kong

    Published 2020
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    Identification of a novel GRIN2D variant in a neonate with intractable epileptic encephalopathy-a case report by Jiancheng Jiao, Li Li, Min Sun, Junchen Fang, Lingzhi Meng, Yudong Zhang, Chao Jia, Li Ma

    Published 2021
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