Search Results - Weixi Li

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    Novel heterozygous compound TRMT5 mutations associated with combined oxidative phosphorylation deficiency 26 in a Chinese family: a case report by Shuiyan Wu, Weixi Li, Zhenjiang Bai, Saihu Huang, Daoping Yang, Hongmei Chen, Ying Li, Ying Liu, Haitao Lv

    Published 2022
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