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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...
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 |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2022
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Materias: | |
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 |
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