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Updated: Jul 15, 2025

Analyses of Proteinuria, Renal Infiltration of Leukocytes, and Renal Deposition of Proteins in Lupus-prone MRL/lpr Mice
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对北欧患者进行基因调查,这些患者患有补充介导脏疾病

Viktor Rydberg1, Sigridur Sunna Aradottir1, Ann-Charlotte Kristoffersson1

  • 1Department of Pediatrics, Clinical Sciences Lund, Lund University, Lund, Sweden.

Frontiers in immunology
|September 25, 2023
PubMed
概括

在141名北欧患者中发现了与补充相关基因的遗传变异,这些患者患有非典型的血溶性尿素性综合征 (aHUS),C3型血球缩性缩症 (C3G) 和免疫复合体介导的膜增殖性血球缩症 (IC-MPGN). 这项研究发现了26种新型变异,强调了对这些罕见脏疾病的基因查的重要性.

关键词:
在C3型淋巴细胞病变中.非典型的血液溶解尿素性尿性综合征.补充补充补充补充补充补充补充.基因 基因 基因 基因膜增殖性球体隆性炎 膜增殖性球体隆性炎

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