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    A novel mutation in the FGG gene causes hypofibrinogenemia in a Chinese family

    A novel mutation in the FGG gene causes hypofibrinogenemia in a Chinese family por Xiaoying Xie, Juan Du, Shunkang Geng, Baoqin Yi, Qingpu Li, Jiangcheng Zuo

    Publicado em 2024-02-01
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