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Comprehensive genetic diagnosis of Japanese patients with severe proteinuria
Numerous disease-causing gene mutations have been identified in proteinuric diseases, such as nephrotic syndrome and glomerulosclerosis. This report describes the results of comprehensive genetic diagnosis of Japanese patients with severe proteinuria. In addition, the report describes the clinical c...
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| 發表在: | Sci Rep |
|---|---|
| Main Authors: | , , , , , , , , , , |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
Nature Publishing Group UK
2020
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| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6959278/ https://ncbi.nlm.nih.gov/pubmed/31937884 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41598-019-57149-5 |
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