Novel heterozygous mutation in COL4A4 responsible for Alport syndrome in a Chinese family
Background: Chronic kidney disease, a global public health problem, results in kidney damage or a gradual decline in the glomerular filtration rate. Alport syndrome is commonly characterized by chronic glomerulonephritis caused by a structural disorder in the glomerular basement membrane. Currently,...
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| Hlavní autoři: | , , , , , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
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Frontiers Media S.A.
2022-09-01
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| Edice: | Frontiers in Genetics |
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| On-line přístup: | https://www.frontiersin.org/articles/10.3389/fgene.2022.899006/full |
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