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Mendeley readers
| Title |
Genetic and clinical peculiarities in a new family with hereditary hypophosphatemic rickets with hypercalciuria: a case report
|
|---|---|
| Published in |
Orphanet Journal of Rare Diseases, January 2010
|
| DOI | 10.1186/1750-1172-5-1 |
| Pubmed ID | |
| Authors |
Natalia Mejia-Gaviria, Helena Gil-Peña, Eliecer Coto, Teresa M Pérez-Menéndez, Fernando Santos |
Mendeley readers
The data shown below were compiled from readership statistics for 1 Mendeley reader of this research output. Click here to see the associated Mendeley record.
Geographical breakdown
| Country | Count | As % |
|---|---|---|
| Japan | 1 | 100% |
| Denmark | 1 | 100% |
Demographic breakdown
| Readers by professional status | Count | As % |
|---|---|---|
| Researcher | 4 | 400% |
| Student > Master | 4 | 400% |
| Student > Bachelor | 4 | 400% |
| Student > Ph. D. Student | 3 | 300% |
| Professor > Associate Professor | 3 | 300% |
| Other | 8 | 800% |
| Readers by discipline | Count | As % |
|---|---|---|
| Medicine and Dentistry | 13 | 1300% |
| Agricultural and Biological Sciences | 6 | 600% |
| Biochemistry, Genetics and Molecular Biology | 3 | 300% |
| Computer Science | 2 | 200% |
| Physics and Astronomy | 1 | 100% |
| Other | 1 | 100% |