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Quantitative Trait Loci Influence Renal Disease Progression in a Mouse Model of Alport Syndrome
Alport syndrome is a human hereditary glomerulonephritis which results in end-stage renal failure (ESRF) in most cases. It is caused by mutations in any one of the collagen α3(IV), α4(IV), or α5(IV) chain genes (COL4A3-COL4A5). Patients carrying identical mutations can exhibit very different disease...
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| Hlavní autoři: | , , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
American Society for Investigative Pathology
2002
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1850644/ https://ncbi.nlm.nih.gov/pubmed/11839593 |
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