Heterozygous laminin β2 mutation in C3 glomerulopathy
C3 glomerulopathy is usually seen with the presence of C3 nephritic factor, homozygous or heterozygous mutations in the regulatory complement proteins factor H, factor I, or C3. We describe the presence of heterozygous laminin β2 mutation in a patient of C3 glomerulonephritis with ocular and central...
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| 主要な著者: | , , , |
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| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Wolters Kluwer Medknow Publications
2021-01-01
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| シリーズ: | Saudi Journal of Kidney Diseases and Transplantation |
| オンライン･アクセス: | http://www.sjkdt.org/article.asp?issn=1319-2442;year=2021;volume=32;issue=5;spage=1479;epage=1481;aulast=Balwani |
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