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    Case report: Heterozygous mutation in HTRA1 causing typical cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy

    Case report: Heterozygous mutation in HTRA1 causing typical cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy 由 Yu-Ming Li, Wei Jia, Tao Xin, Tao Xin, Tao Xin, Tao Xin, Yu-Qing Fang, Yu-Qing Fang

    出版 2023-09-01
    主题: “...cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy...”
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