Genotype-phenotype correlation of WT1 mutation-related nephropathy in Chinese children

INTRODUCTION: This study aimed to analyze the clinical characteristics of nephropathy associated with WT1 gene mutations in Chinese children and explore the relationship between genotype and clinical phenotype. METHODS: Cases diagnosed at the Guangzhou Women and Children's Medical Center, were...

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Detalles Bibliográficos
Autores principales: Chen, Huanru, Zhang, Miao, Lin, Jinai, Lu, Jieyi, Zhong, Fazhan, Zhong, Fu, Gao, Xia, Liao, Xin
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/PMC10416235/
https://www.ncbi.nlm.nih.gov/pubmed/37576146
http://dx.doi.org/10.3389/fped.2023.1192021

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10416235/
https://www.ncbi.nlm.nih.gov/pubmed/37576146
http://dx.doi.org/10.3389/fped.2023.1192021

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