| Title |
A novel CLCNKB mutation in a Chinese girl with classic Bartter syndrome: a case report
|
|---|---|
| Published in |
BMC Medical Genomics, August 2019
|
| DOI | 10.1186/s12881-019-0869-9 |
| Pubmed ID | |
| Authors |
Binlu Zhu, Hong Jiang, Meiling Cao, Xueqi Zhao, Hongkun Jiang |
Mendeley readers
The data shown below were compiled from readership statistics for 22 Mendeley readers of this research output. Click here to see the associated Mendeley record.
Geographical breakdown
| Country | Count | As % |
|---|---|---|
| Unknown | 22 | 100% |
Demographic breakdown
| Readers by professional status | Count | As % |
|---|---|---|
| Student > Doctoral Student | 2 | 9% |
| Professor > Associate Professor | 2 | 9% |
| Student > Ph. D. Student | 2 | 9% |
| Unspecified | 1 | 5% |
| Student > Bachelor | 1 | 5% |
| Other | 2 | 9% |
| Unknown | 12 | 55% |
| Readers by discipline | Count | As % |
|---|---|---|
| Medicine and Dentistry | 6 | 27% |
| Psychology | 2 | 9% |
| Agricultural and Biological Sciences | 1 | 5% |
| Unspecified | 1 | 5% |
| Biochemistry, Genetics and Molecular Biology | 1 | 5% |
| Other | 1 | 5% |
| Unknown | 10 | 45% |