Multicenter study of the clinical features and mutation gene spectrum of Chinese children with Dent disease-Reference-Cited by-全球学者库

Multicenter study of the clinical features and mutation gene spectrum of Chinese children with Dent disease

Published:2020-01-13 Issue:3 Volume:97 Page:407-417
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:Clin Genet

Author:

Ye Qing¹,Shen Qian²³⁴,Rao Jia²³⁴^ORCID,Zhang Aihua⁵^ORCID,Zheng Bixia⁶,Liu Xiaorong⁷⁸,Shen Ying⁷⁸,Chen Zhi⁷⁸,Wu Yubing⁹,Hou Ling⁹,Jian Shan¹⁰,Wei Min¹⁰,Ma Mingsheng¹⁰,Sun Shuzhen¹¹,Li Qian¹¹,Dang Xiqiang¹²,Wang Ying¹²,Xu Hong²³⁴,Mao Jianhua¹^ORCID,

Affiliation:

1. Department of NephrologyThe Children's Hospital, Zhejiang University School of Medicine, National clinical research center for child health Hangzhou China

2. Department of NephrologyChildren's Hospital of Fudan University Shanghai China

3. Shanghai Kidney Development and Pediatric Kidney Disease Research Center Shanghai China

4. Shanghai Key Lab of Birth Defect, Children's Hospital of Fudan University Shanghai China

5. Department of NephrologyNanjing Children's Hospital Affiliated to Nanjing Medical University Nanjing China

6. Nanjing Key Laboratory of Pediatrics, Children's Hospital of Nanjing Medical University Nanjing China

7. Department of NephrologyBejing Children's Hospital Affiliated to Capital University of Medical Science Beijing China

8. Beijing Children's Key Laboratory of Chronic Kidney Disease and Blood Purification Beijing China

9. Department of Pediatric Nephrology and RheumatologyShengfing Hospital of China Medical University Shenyang China

10. Department of PediatricsPeking Union Medical College Hospital Beijing China

11. Department of PediatricNephrology, Rheumatism and Immunology, Shandong Provincial Hospital Jinan China

12. Department of PediatricXiangya Hospital Central South University Changsha China

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/cge.13663

Reference48 articles.

1. Renal manifestations of Dent disease and Lowe syndrome

2. Hypercalcuric Rickets Associated with Renal Tubular Damage

3. Genetic spectrum of renal disease for 1001 Chinese children based on a multicenter registration system

4. Phenotypic and genetic heterogeneity in Dent's disease—the results of an Italian collaborative study

5. Urinary phosphate/creatinine, calcium/creatinine, and magnesium/creatinine ratios in a healthy pediatric population

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