Genetic spectrum of CAKUT and risk factors for kidney failure: a paediatric multicentre cohort study

BACKGROUND: Congenital anomalies of the kidney and urinary tract (CAKUT) are the leading cause of kidney failure in children with phenotypic and genotypic heterogeneity. Our objective was to describe the genetic spectrum and identify the risk factors for kidney failure in children with CAKUT. METHOD...

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Detalles Bibliográficos
Autores principales: Liu, Jia-Lu, Wang, Xiao-Wen, Liu, Cui-Hua, , Duan Ma, Gao, Xiao-Jie, Jiang, Xiao-Yun, Mao, Jian-Hua, Zhu, Guang-Hua, Zhang, Ai-Hua, Wang, Mo, Dang, Xi-Qiang, Zhuang, Jie-Qiu, Li, Yu-Feng, Bai, Hai-Tao, Zhang, Rui-Feng, Shen, Tong, Bi, Yun-Li, Sun, Yu-Bo, Wang, Xiang, Wu, Bing-Bing, Chen, Jing, Rao, Jia, Tang, Xiao-Shan, Shen, Qian, Xu, Hong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10468753/
https://www.ncbi.nlm.nih.gov/pubmed/36549658
http://dx.doi.org/10.1093/ndt/gfac338

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10468753/
https://www.ncbi.nlm.nih.gov/pubmed/36549658
http://dx.doi.org/10.1093/ndt/gfac338

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