尿MCP

Marina Noris1, Simona Brioschi, Jessica Caprioli

  • 1Mario Negri Institute for Pharmacological Research, Clinical Research Center for Rare Diseases, Aldo e Cele Daccò, Villa Camozzi-Ranica, Bergamo, Italy. noris@marionegri.it

Lancet (London, England)
|November 15, 2003
PubMed
概括

膜辅因子蛋白 (MCP) 的突变在家族性腹阴性血溶性尿素综合征 (D-HUS) 病例中被发现. 这表明受损的补体调节有助于D-HUS,涉及MCP作为潜在的遗传原因.

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