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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| Hlavní autoři: | , , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Wolters Kluwer Medknow Publications
2021-01-01
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| Edice: | Saudi Journal of Kidney Diseases and Transplantation |
| On-line přístup: | 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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