A novel CLCN5 frame shift mutation responsible for Dent disease 1: Case report.

Ni, Jiajia; Zhu, Yaju; Lin, Fujun; Guan, Wenbin; Jin, Jing; Li, Yufeng; Guo, Guimei

Ni, Jiajia; Zhu, Yaju; Lin, Fujun; Guan, Wenbin; Jin, Jing; Li, Yufeng; Guo, Guimei.

Afiliación

Ni J; Department of Pediatric Nephrology, Rheumatology and Immunology, Xinhua Hospital Affiliated to Shanghai Jiaotong University School of Medicine, Shanghai, China.
Zhu Y; Department of Pediatric Nephrology, Rheumatology and Immunology, Xinhua Hospital Affiliated to Shanghai Jiaotong University School of Medicine, Shanghai, China.
Lin F; Department of Nephrology, Xin Hua Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, China.
Guan W; Department of Pathology, Xin Hua Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, China.
Jin J; Department of Pediatric Nephrology, Rheumatology and Immunology, Xinhua Hospital Affiliated to Shanghai Jiaotong University School of Medicine, Shanghai, China.
Li Y; Department of Pediatric Nephrology, Rheumatology and Immunology, Xinhua Hospital Affiliated to Shanghai Jiaotong University School of Medicine, Shanghai, China.
Guo G; Department of Pediatric Nephrology, Rheumatology and Immunology, Xinhua Hospital Affiliated to Shanghai Jiaotong University School of Medicine, Shanghai, China.

Front Pediatr ; 10: 1043502, 2022.

Article en En | MEDLINE | ID: mdl-36452359

Palabras clave

CLCN5 gene mutation; Dent disease; X-link; low molecular weight proteinuria; renal tubule disorders

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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: Front Pediatr Año: 2022 Tipo del documento: Article País de afiliación: China Pais de publicación: Suiza

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