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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Detalles Bibliográficos
Autores principales: Zhang, Li, Sun, Bai-chao, Zhao, Bing-gang, Ma, Qing-shan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Research Article
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

Internet

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

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