Characteristics of Allan-Herndon-Dudley Syndrome in Chinese children: Identification of two novel pathogenic variants of the SLC16A2 gene by Qiang Zhang, Qi Yang, Xunzhao Zhou, Zailong Qin, Shang Yi, Jingsi Luo

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Clinical features and molecular genetic investigation of infantile-onset ascending hereditary spastic paralysis (IAHSP) in two Chinese siblings caused by a novel splice site ALS2 v... by Qiang Zhang, Qi Yang, Jingsi Luo, Xunzhao Zhou, Shang Yi, Shuyin Tan, Zailong Qin

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Novel loss-of-function variants in WDR26 cause Skraban-Deardorff syndrome in two Chinese patients by Qi Yang, Qi Yang, Xunzhao Zhou, Xunzhao Zhou, Sheng Yi, Sheng Yi, XiaoLing Li, Qiang Zhang, Qiang Zhang, Shujie Zhang, Shujie Zhang, Li Lin, Li Lin, Shang Yi, Shang Yi, Biyan Chen, Biyan Chen, Zailong Qin, Zailong Qin, Jingsi Luo, Jingsi Luo, Jingsi Luo

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