Search Results - Caishi Liao

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    A Chinese patient with developmental and epileptic encephalopathies (DEE) carrying a TRPM3 gene mutation: a paediatric case report by Qingyun Kang, Liming Yang, Hongmei Liao, Sai Yang, Xiaojun Kuang, Zeshu Ning, Caishi Liao, Bo Chen

    Published 2021
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    Case Report: Compound Heterozygous Variants of SLC13A3 Identified in a Chinese Patient With Acute Reversible Leukoencephalopathy and α-Ketoglutarate Accumulation by Qingyun Kang, Liming Yang, Hongmei Liao, Sai Yang, Haiyang Yang, Zeshu Ning, Caishi Liao, Liwen Wu

    Published 2021
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