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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...
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| Publicado no: | BMC Nephrol |
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| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7379802/ https://ncbi.nlm.nih.gov/pubmed/32703181 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12882-020-01962-y |
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