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Case report: a Chinese girl with dent disease 1 and turner syndrome due to a hemizygous CLCN5 gene mutation and Isochromosome (Xq)

Overview of attention for article published in BMC Nephrology, May 2020
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Title
Case report: a Chinese girl with dent disease 1 and turner syndrome due to a hemizygous CLCN5 gene mutation and Isochromosome (Xq)
Published in
BMC Nephrology, May 2020
DOI 10.1186/s12882-020-01827-4
Pubmed ID
Authors

Yuhong Ye, Jingjing Wang, Xiaofang Quan, Ke Xu, Haidong Fu, Weiyue Gu, Jianhua Mao

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 7 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 7 100%

Demographic breakdown

Readers by professional status Count As %
Student > Master 1 14%
Student > Postgraduate 1 14%
Unknown 5 71%
Readers by discipline Count As %
Agricultural and Biological Sciences 1 14%
Medicine and Dentistry 1 14%
Unknown 5 71%