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Mendeley readers
| Title |
Phenotypic variability and identification of novel YARS2 mutations in YARS2 mitochondrial myopathy, lactic acidosis and sideroblastic anaemia
|
|---|---|
| Published in |
Orphanet Journal of Rare Diseases, December 2013
|
| DOI | 10.1186/1750-1172-8-193 |
| Pubmed ID | |
| Authors |
Lisa G Riley, Minal J Menezes, Joëlle Rudinger-Thirion, Rachael Duff, Pascale de Lonlay, Agnes Rotig, Michel C Tchan, Mark Davis, Sandra T Cooper, John Christodoulou |
Mendeley readers
The data shown below were compiled from readership statistics for 37 Mendeley readers of this research output. Click here to see the associated Mendeley record.
Geographical breakdown
| Country | Count | As % |
|---|---|---|
| Unknown | 37 | 100% |
Demographic breakdown
| Readers by professional status | Count | As % |
|---|---|---|
| Student > Ph. D. Student | 11 | 30% |
| Researcher | 3 | 8% |
| Professor | 2 | 5% |
| Student > Bachelor | 2 | 5% |
| Student > Doctoral Student | 1 | 3% |
| Other | 5 | 14% |
| Unknown | 13 | 35% |
| Readers by discipline | Count | As % |
|---|---|---|
| Biochemistry, Genetics and Molecular Biology | 6 | 16% |
| Medicine and Dentistry | 6 | 16% |
| Neuroscience | 2 | 5% |
| Arts and Humanities | 1 | 3% |
| Psychology | 1 | 3% |
| Other | 3 | 8% |
| Unknown | 18 | 49% |