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  1. Article

    Open Access

    A novel homozygous variant of GPR98 causes usher syndrome type IIC in a consanguineous Chinese family by next generation sequencing

    Usher syndrome (USH) is a common heterogeneous retinopathy and a hearing loss (HL) syndrome. However, the gene causing Usher syndrome type IIC (USH2C) in a consanguineous Chinese pedigree is unknown.

    Chunli Wei, Lisha Yang, **gliang Cheng, Saber Imani, Shangyi Fu… in BMC Medical Genetics (2018)

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  2. No Access

    Article

    In vitro and in vivo activity of ceftazidime/avibactam and aztreonam alone or in combination against mcr-9, serine- and metallo-β-lactamases–co-producing carbapenem-resistant Enterobacter cloacae complex

    Enterobacteriaceae carrying mcr-9, in particularly those also co-containing metallo-β-lactamase (MBL) and TEM type β-lactamase, present potential transmission risks and lack adequate clinical response methods, th...

    Wengang Li, Jisheng Zhang, Yanjun Fu… in European Journal of Clinical Microbiology … (2024)