Clinical features and gene variation analysis of COQ8B nephropathy: Report of seven cases

OBJECTIVE: COQ8B nephropathy is a relatively rare autosomal recessive kidney disease characterized by proteinuria and a progressive deterioration of renal function, eventually leading to end-stage renal disease (ESRD). The objective is to study the characteristics and correlation between the genotyp...

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Detalles Bibliográficos
Autores principales: Liang, Rui, Chen, Xuelan, Zhang, Ying, Law, Chak-Fun, Yu, Sijie, Jiao, Jia, Yang, Qin, Wu, Daoqi, Zhang, Gaofu, Chen, Han, Wang, Mo, Yang, Haiping, Wang, Anshuo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Pediatrics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9948246/
https://www.ncbi.nlm.nih.gov/pubmed/36843884
http://dx.doi.org/10.3389/fped.2022.1030191

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9948246/
https://www.ncbi.nlm.nih.gov/pubmed/36843884
http://dx.doi.org/10.3389/fped.2022.1030191

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