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Mendeley readers
| Title |
Pediatric patients with RASopathy-associated hypertrophic cardiomyopathy: the multifaceted consequences of PTPN11 mutations
|
|---|---|
| Published in |
Orphanet Journal of Rare Diseases, July 2019
|
| DOI | 10.1186/s13023-019-1151-0 |
| Pubmed ID | |
| Authors |
Giulio Calcagni, Maria Cristina Digilio, Bruno Marino, Marco Tartaglia |
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 % |
|---|---|---|
| Researcher | 4 | 18% |
| Student > Bachelor | 3 | 14% |
| Other | 2 | 9% |
| Student > Postgraduate | 2 | 9% |
| Professor | 1 | 5% |
| Other | 2 | 9% |
| Unknown | 8 | 36% |
| Readers by discipline | Count | As % |
|---|---|---|
| Medicine and Dentistry | 6 | 27% |
| Biochemistry, Genetics and Molecular Biology | 4 | 18% |
| Agricultural and Biological Sciences | 2 | 9% |
| Social Sciences | 1 | 5% |
| Unspecified | 1 | 5% |
| Other | 0 | 0% |
| Unknown | 8 | 36% |