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Mendeley readers
| Title |
Rare recessive loss-of-function methionyl-tRNA synthetase mutations presenting as a multi-organ phenotype
|
|---|---|
| Published in |
BMC Medical Genomics, October 2013
|
| DOI | 10.1186/1471-2350-14-106 |
| Pubmed ID | |
| Authors |
Eline van Meel, Daniel J Wegner, Paul Cliften, Marcia C Willing, Frances V White, Stuart Kornfeld, F Sessions Cole |
Mendeley readers
The data shown below were compiled from readership statistics for 52 Mendeley readers of this research output. Click here to see the associated Mendeley record.
Geographical breakdown
| Country | Count | As % |
|---|---|---|
| Spain | 1 | 2% |
| France | 1 | 2% |
| Germany | 1 | 2% |
| Unknown | 49 | 94% |
Demographic breakdown
| Readers by professional status | Count | As % |
|---|---|---|
| Researcher | 11 | 21% |
| Student > Master | 10 | 19% |
| Student > Ph. D. Student | 8 | 15% |
| Other | 6 | 12% |
| Student > Doctoral Student | 1 | 2% |
| Other | 4 | 8% |
| Unknown | 12 | 23% |
| Readers by discipline | Count | As % |
|---|---|---|
| Agricultural and Biological Sciences | 11 | 21% |
| Medicine and Dentistry | 10 | 19% |
| Biochemistry, Genetics and Molecular Biology | 10 | 19% |
| Pharmacology, Toxicology and Pharmaceutical Science | 2 | 4% |
| Neuroscience | 2 | 4% |
| Other | 6 | 12% |
| Unknown | 11 | 21% |