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Establishment of X-linked Alport syndrome model mice with a Col4a5 R471X mutation
Alport syndrome (AS) is an inherited disorder characterized by glomerular basement membrane (GBM) abnormality and development of chronic kidney disease at an early age. The cause of AS is a genetic mutation in type IV collagen, and more than 80% of patients have X-linked AS (XLAS) with mutation in C...
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| 出版年: | Biochem Biophys Rep |
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| 主要な著者: | , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Elsevier
2018
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6295608/ https://ncbi.nlm.nih.gov/pubmed/30582011 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.bbrep.2018.12.003 |
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