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An overview of the multi-pronged approach in the diagnosis of Alport syndrome for 22 children in Northeast China
BACKGROUND: Alport syndrome (AS) is a kind of progressive hereditary nephritis induced by mutations of different genes that encode collagen IV. The affected individuals usually develop hematuria during childhood, accompanying with gradual deterioration of renal functions. In this study, the multi-pr...
| Autores principales: | , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
BioMed Central
2020
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7379802/ https://www.ncbi.nlm.nih.gov/pubmed/32703181 http://dx.doi.org/10.1186/s12882-020-01962-y |