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校正: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 9, 2024
PubMed
概括

这项研究纠正了之前的一篇文章DOI. 更新的信息确保准确的引用和检索免疫学研究结果.

科学领域:

  • 免疫学 免疫学 免疫学
  • 科学出版科学出版
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 基因这是一种膜增殖性球性炎 (glomerulonephritis).

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A complementation test is a simple cross to identify whether the two mutations are located on the same gene or different genes. It was first performed by Edward Lewis in the 1940s while working on fruit flies. He developed the test to identify the location and arrangement of different mutations on chromosomes.
Organisms heterozygous for different mutations are crossed pairwise in all combinations. If present on different genes, the mutations can complement each other by providing the missing...
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