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Mendeley readers
| Title |
A de novo SCN8A heterozygous mutation in a child with epileptic encephalopathy: a case report
|
|---|---|
| Published in |
BMC Pediatrics, November 2019
|
| DOI | 10.1186/s12887-019-1796-9 |
| Pubmed ID | |
| Authors |
Kao-Min Lin, Geng Su, Fengpeng Wang, Xiaobin Zhang, Yuanqing Wang, Jun Ren, Xin Wang, Yi Yao, Ying Zhou |
Mendeley readers
The data shown below were compiled from readership statistics for 15 Mendeley readers of this research output. Click here to see the associated Mendeley record.
Geographical breakdown
| Country | Count | As % |
|---|---|---|
| Unknown | 15 | 100% |
Demographic breakdown
| Readers by professional status | Count | As % |
|---|---|---|
| Other | 3 | 20% |
| Student > Bachelor | 3 | 20% |
| Unspecified | 1 | 7% |
| Student > Ph. D. Student | 1 | 7% |
| Student > Master | 1 | 7% |
| Other | 2 | 13% |
| Unknown | 4 | 27% |
| Readers by discipline | Count | As % |
|---|---|---|
| Neuroscience | 5 | 33% |
| Medicine and Dentistry | 2 | 13% |
| Nursing and Health Professions | 1 | 7% |
| Agricultural and Biological Sciences | 1 | 7% |
| Unspecified | 1 | 7% |
| Other | 0 | 0% |
| Unknown | 5 | 33% |