Showing 1 - 2 results of 2 for search 'Linyan Zhu', query time: 0.03s Refine Results
  1. 1
    Case report: A compound heterozygous mutations in ASNS broadens the spectrum of asparagine synthetase deficiency in the prenatal diagnosis

    Case report: A compound heterozygous mutations in ASNS broadens the spectrum of asparagine synthetase deficiency in the prenatal diagnosis by Linyan Zhu, Linyan Zhu, Yixi Sun, Yixi Sun, Yuqing Xu, Yuqing Xu, Pengzhen Jin, Pengzhen Jin, Huiqing Ding, Minyue Dong, Minyue Dong

    Published 2023
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  2. 2
    Limb girdle muscular dystrophy 23 caused by compound heterozygous mutations of LAMA2 gene

    Limb girdle muscular dystrophy 23 caused by compound heterozygous mutations of LAMA2 gene by Yuqing Xu, Yuqing Xu, Linyan Zhu, Yeqing Qian, Yeqing Qian, Minyue Dong, Minyue Dong

    Published 2023
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