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Mendeley readers
| Title |
Novel MNX1 mutations and genotype–phenotype analysis of patients with Currarino syndrome
|
|---|---|
| Published in |
Orphanet Journal of Rare Diseases, June 2020
|
| DOI | 10.1186/s13023-020-01442-4 |
| Pubmed ID | |
| Authors |
Lu Han, Zhen Zhang, Hui Wang, Hui Song, Qing Gao, Yuchun Yan, Ran Tao, Ping Xiao, Long Li, Qian Jiang, Qi Li |
Mendeley readers
The data shown below were compiled from readership statistics for 11 Mendeley readers of this research output. Click here to see the associated Mendeley record.
Geographical breakdown
| Country | Count | As % |
|---|---|---|
| Unknown | 11 | 100% |
Demographic breakdown
| Readers by professional status | Count | As % |
|---|---|---|
| Student > Master | 3 | 27% |
| Researcher | 2 | 18% |
| Student > Doctoral Student | 1 | 9% |
| Student > Ph. D. Student | 1 | 9% |
| Unknown | 4 | 36% |
| Readers by discipline | Count | As % |
|---|---|---|
| Medicine and Dentistry | 4 | 36% |
| Biochemistry, Genetics and Molecular Biology | 2 | 18% |
| Environmental Science | 1 | 9% |
| Unknown | 4 | 36% |