Genotype-phenotype correlation of <i>WT1</i> mutation-related nephropathy in Chinese children.

Chen, Huanru; Zhang, Miao; Lin, Jinai; Lu, Jieyi; Zhong, Fazhan; Zhong, Fu; Gao, Xia; Liao, Xin

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

Chen, Huanru; Zhang, Miao; Lin, Jinai; Lu, Jieyi; Zhong, Fazhan; Zhong, Fu; Gao, Xia; Liao, Xin.

Afiliação

Chen H; Department of Nephrology, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, Guangzhou, China.
Zhang M; Department of Nephrology, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, Guangzhou, China.
Lin J; Department of Nephrology, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, Guangzhou, China.
Lu J; Department of Nephrology, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, Guangzhou, China.
Zhong F; Department of Nephrology, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, Guangzhou, China.
Zhong F; Department of Nephrology, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, Guangzhou, China.
Gao X; Department of Nephrology, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, Guangzhou, China.
Liao X; Department of Nephrology, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, Guangzhou, China.

Front Pediatr ; 11: 1192021, 2023.

Article em En | MEDLINE | ID: mdl-37576146

Palavras-chave

Denys-Drash syndrome; Frasier syndrome; WT1 gene; end-stage renal disease; hereditary nephropathy; steroid-resistant nephrotic syndrome

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Front Pediatr Ano de publicação: 2023 Tipo de documento: Article País de afiliação: China

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