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A Comparative Presentation of Mouse Models That Recapitulate Most Features of Alport Syndrome
Alport syndrome is a hereditary kidney disease caused by mutations in the three genes encoding for collagen IV: COL4A3, COL4A4, and COL4A5. Several mouse models have been created for the study of this disease with variable phenotypic outcomes. This review is an up-to-date presentation of the current...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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MDPI
2022
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9601682/ https://www.ncbi.nlm.nih.gov/pubmed/36292778 http://dx.doi.org/10.3390/genes13101893 |